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GENE - TERM ANNOTATION REPORT

338 Annotations Found.

An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Young SG, etal., J Clin Invest. 1987 Jun;79(6):1842-51.
  • 2 additional annotations were made from Young SG, etal., J Clin Invest. 1987 Jun;79(6):1842-51.
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Qualifier: susceptibility

  • This annotation was curated on 2018-05-05 09:00:47.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred from expression pattern (IEP)
  •  
  • The annotation was made from Clarke MW, etal., Clin Chem. 2006 Jul;52(7):1339-45. Epub 2006 May 25.
  • 2 additional annotations were made from Clarke MW, etal., Clin Chem. 2006 Jul;52(7):1339-45. Epub 2006 May 25.
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: protein:decreased expression:plasma

  • This annotation was curated on 2018-05-05 09:00:48.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11593325 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:26.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11560425 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:14:13.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8566422 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:12124991

  • This annotation was curated on 2020-03-26 10:13:58.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8600802 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:2022744

  • This annotation was curated on 2020-03-26 10:14:59.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11579905 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:17:58.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11578687 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:22.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11578933 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:10.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11578331 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:15:49.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11580870 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:36.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11586614 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:43.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11579241 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:16:14.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11586505 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:18:59.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11578735 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:20.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11656850 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:18:14.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11579529 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:16:15.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11580254 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:24033266, PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:36.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11650801 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:18:16.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11654273 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:19:15.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11347377 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:42.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11560460 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:57.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11544878 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:18.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11544494 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:13.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8659007 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:16:38.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10449684 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:26467025, PMID:27765764, PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:36.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13437451 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:14:38.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8659009 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:16:39.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8659013 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:16:39.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11584483 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:19:10.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11580336 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:17:56.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8570409 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:21981844

  • This annotation was curated on 2020-03-26 10:16:48.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11579559 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:17:36.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11579152 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:17:01.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11647351 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:17:57.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11547871 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:27765764, PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:53.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11560396 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:16:48.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11580791 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:17:22.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11644637 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:18:16.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11578630 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:17:03.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11652299 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:19:31.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11579743 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:17:25.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8600800 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:2312735, PMID:2725600

  • This annotation was curated on 2020-03-26 10:14:59.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8659012 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:16:39.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11644915 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:18:45.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8566420 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:1454832, PMID:221546

  • This annotation was curated on 2020-03-26 10:13:58.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11589398 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:19:01.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8600795 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:2843815

  • This annotation was curated on 2020-03-26 10:14:59.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8659003 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:24033266, PMID:25741868

  • This annotation was curated on 2020-03-26 10:16:38.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11652991 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:19:21.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11652679 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:18:31.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13216030 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:18:14.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11543801 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:18:24.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13437356 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:14:10.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11653560 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:18:18.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11646545 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:19:04.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11581094 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:18:19.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8659005 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:16:38.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11578159 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:18:15.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13437446 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:14:33.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11092609 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Hypobetalipoproteinemia
  • Original References(s): PMID:24033266, PMID:24751931, PMID:25335495

  • This annotation was curated on 2020-03-26 10:18:13.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8600799 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:8792774

  • This annotation was curated on 2020-03-26 10:14:59.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11644267 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:19:14.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11652970 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:19:21.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11589982 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:17:13.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10406669 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:13:41.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11653719 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:18:34.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11584495 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:19:23.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11588392 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:19:12.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11645602 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:18:14.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13437481 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:18:15.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13214749 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:18:43.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8600798 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:2725600, PMID:2843815

  • This annotation was curated on 2020-03-26 10:14:59.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11585457 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:18:41.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11587314 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:18:55.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11579182 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:17:11.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8566421 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:11940084

  • This annotation was curated on 2020-03-26 10:13:58.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11588636 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:16:03.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11525916 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:57.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11579665 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:17:57.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8600793 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:1454832, PMID:221546, PMID:3399894, PMID:3473077

  • This annotation was curated on 2020-03-26 10:14:58.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11593393 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:19:08.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11651220 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:19:22.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11547255 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:37.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11590636 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:18:42.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11583648 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:19:34.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11652640 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:19:27.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8566418 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:2567736

  • This annotation was curated on 2020-03-26 10:13:58.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8600804 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:1562615

  • This annotation was curated on 2020-03-26 10:14:59.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11577640 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:18:34.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8600794 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:2843815

  • This annotation was curated on 2020-03-26 10:14:59.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11583473 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:19:31.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11579916 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:17:58.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11577869 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:18:18.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11580655 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia

  • This annotation was curated on 2020-03-26 10:17:36.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11347882 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:11.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13476921 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:48.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13803117 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:54.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626662 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:02.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13470234 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:19.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13480129 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:23054246, PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:57.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8600806 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:11031227, PMID:15797858, PMID:17046772, PMID:17160438, PMID:17588943, PMID:17595251, PMID:17968143, PMID:18022922, PMID:18028451, PMID:18160469, PMID:18222178, PMID:18258526, PMID:18279815, PMID:18325181, PMID:18355452, PMID:22923420, PMID:23375686, PMID:24033266, PMID:24607922, PMID:25741868, PMID:26332594, PMID:26802169, PMID:28492532, PMID:28965616, PMID:29572815, PMID:7883971, PMID:9105560, PMID:9603795, PMID:9925662

  • This annotation was curated on 2020-03-26 10:15:24.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14714279 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:27.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14707387 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:20657596, PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:43.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14731506 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:25.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14703637 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:05.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14721676 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:37.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13467922 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:02.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14714290 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:27.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11578859 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:51.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13472849 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:55.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14724575 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:48.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14690545 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:01.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14742582 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:45.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13211316 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:28.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14716163 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:32.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626637 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:02.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11543366 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:21.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626601 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:02.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13497089 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:16.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13211304 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:27.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11585539 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:19:25.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11584935 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:40.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11578826 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:43.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13490090 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:24.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11587021 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:52.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12741880 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:19:32.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11589107 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:58.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11581183 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:26.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11584317 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:19.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11635458 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:19.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11578653 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:13.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11587736 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:17:45.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11589949 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:19:15.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11582674 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:18:31.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11579145 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:17:00.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8630156 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:29.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11592440 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:19:06.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11580366 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:00.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11591852 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:58.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11656897 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:33.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11578469 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:22.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8659004 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:15:04.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11578683 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:18.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11578482 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:30.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11583268 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:43.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11578549 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:45.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13473388 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:42.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13802536 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:42.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13495808 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:42.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12891085 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:19:24.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14708508 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:39.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626632 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:10.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13482817 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:08.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13704328 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:26.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626590 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:57.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626646 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:11.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626651 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:12.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13805808 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:24507775, PMID:28492532, PMID:8468533

  • This annotation was curated on 2020-03-26 10:15:34.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14722066 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:25.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14721509 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:05.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14741544 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:28.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13817319 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:03.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11579777 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:13.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14736507 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:36.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12741245 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:19:26.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14729959 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:25.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626660 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:23.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13506317 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:14:44.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11577484 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:26467025

  • This annotation was curated on 2020-03-26 10:16:09.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13513059 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:51.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12896498 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:22923420, PMID:24033266, PMID:24503134, PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:13.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13817160 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:59.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11560406 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:55.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11543897 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:26.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13807912 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:41.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13812520 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:30.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14707299 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:57.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8659006 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:21408211, PMID:25741868, PMID:26467025, PMID:28492532, PMID:8960785

  • This annotation was curated on 2020-03-26 10:16:38.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12889944 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:19:13.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14718549 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:57.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626629 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:10.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13500995 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:15.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626597 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:57.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626640 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:11.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626600 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:57.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626644 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:11.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626648 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:12.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13815786 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:35.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626654 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:12.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13478128 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:57.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11589851 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:16.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11544513 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:14.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10449839 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:56.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14713009 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:34.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626647 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:11.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11548997 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:37.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626598 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:57.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626658 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:23.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626608 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:36.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14726811 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:40.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13806831 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:55.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14737891 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:06.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14738027 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:37.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8600797 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:1424233, PMID:1602000, PMID:2574033

  • This annotation was curated on 2020-03-26 10:14:59.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11348514 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:57.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10449812 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:17:54.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11590763 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:57.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12889443 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:19:28.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13512019 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:56.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14713770 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:02.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14689939 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:55.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11578284 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:43.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13821750 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:30.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14728502 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:17.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626664 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:23.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13810095 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:17.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10046843 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:26036859, PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:37.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13806496 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:07.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11560429 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:12.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13498543 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:41.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12885031 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:52.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8625283 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:44.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626592 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:57.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626599 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:57.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626605 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:58.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626609 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:58.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626602 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:57.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626603 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:58.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12884452 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:49.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626656 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:12.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14723685 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:10.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626606 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:58.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8625280 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:22408029, PMID:24033266, PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:43.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626586 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:56.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626610 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:58.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13817408 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:24.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626587 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:56.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626591 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:57.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626649 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:13.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626650 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:12.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8600796 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:1424233, PMID:2574033

  • This annotation was curated on 2020-03-26 10:14:59.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13494618 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:25.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626633 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:10.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13812464 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:09.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13469247 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:45.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626636 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:11.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626652 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:12.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13477359 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:40.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11579803 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:28.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13822388 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Hypobetalipoproteinemia
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:33.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11589357 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:18:16.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626661 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:23.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11577934 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:31.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11580130 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:55.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13811759 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:32.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11593464 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:43.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14724568 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:26.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11634728 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:17:01.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13818495 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:35.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626666 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:24.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13815753 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:33.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626659 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:23.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13813779 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:22095935, PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:15.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11582383 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:19:05.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626635 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:10.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11579373 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:20.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11592198 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:19:04.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13483465 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:47.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11579624 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:47.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14741675 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:49.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11589923 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:19:02.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8600805 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:2903181

  • This annotation was curated on 2020-03-26 10:14:59.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12896703 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:16250003, PMID:20506408, PMID:24033266, PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:21.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626630 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:10.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13812121 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:18325181, PMID:20828696, PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:01.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11578836 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:16:46.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11580946 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:18.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626594 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:57.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13479930 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:06.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13815788 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:35.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11591396 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:18:20.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8659008 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:22095935, PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:38.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8600801 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Hypobetalipoproteinemia
  • Original References(s): PMID:10208479, PMID:10388479, PMID:10735632, PMID:10952765, PMID:11115503, PMID:11137107, PMID:11494965, PMID:11781700, PMID:11810272, PMID:1360085, PMID:1466657, PMID:1493642, PMID:15797858, PMID:1600334, PMID:17142622, PMID:17160438, PMID:17539906, PMID:17765246, PMID:1793440, PMID:18028451, PMID:18096825, PMID:18222178, PMID:18325181, PMID:18700895, PMID:1977310, PMID:20145306, PMID:20236128, PMID:20736250, PMID:20809525, PMID:21059979, PMID:21310417, PMID:21382890, PMID:21657943, PMID:21868016, PMID:21919778, PMID:22244043, PMID:22698793, PMID:2280177, PMID:22883975, PMID:23054246, PMID:23064986, PMID:23130880, PMID:23375686, PMID:2375782, PMID:24033266, PMID:24106285, PMID:24234650, PMID:24404629, PMID:24507774, PMID:24956927, PMID:24987033, PMID:25461735, PMID:2563166, PMID:25741868, PMID:26036859, PMID:26415676, PMID:26467025, PMID:26636822, PMID:26643808, PMID:27765764, PMID:28492532, PMID:3477815, PMID:3771801, PMID:7627691, PMID:7883971, PMID:8141833, PMID:8254047, PMID:8318509, PMID:8318993, PMID:8371062, PMID:8478017, PMID:8723684, PMID:8831935, PMID:9081691, PMID:9104431, PMID:9105560, PMID:9259199, PMID:9339363, PMID:9603795, PMID:9654205

  • This annotation was curated on 2020-03-26 10:14:59.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11592150 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:46.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14726478 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:21520333, PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:02.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13704334 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:24.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14709811 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:29.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11650919 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:19:18.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11588112 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:01.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11588620 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:01.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11585560 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:19:32.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11633625 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:27765764

  • This annotation was curated on 2020-03-26 10:16:46.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11577570 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:18:23.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11579127 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:16:56.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11349042 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:14.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14709712 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:11.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11581075 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:15.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11579646 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:53.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11593750 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:19:08.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13805034 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:33.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13812882 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:20032471, PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:26.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14690914 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:14.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8659010 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532, PMID:7670940, PMID:8960785

  • This annotation was curated on 2020-03-26 10:16:39.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11347334 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:10388479, PMID:10529757, PMID:11238294, PMID:11833852, PMID:16250003, PMID:17964958, PMID:20538126, PMID:21376320, PMID:21862702, PMID:22294733, PMID:22353362, PMID:23375686, PMID:23936638, PMID:24033266, PMID:24234650, PMID:24784157, PMID:2563166, PMID:25741868, PMID:26415676, PMID:27206935, PMID:27765764, PMID:27783906, PMID:28492532, PMID:7627691, PMID:9191540, PMID:9702952

  • This annotation was curated on 2020-03-26 10:17:16.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8630158 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:29.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12888084 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:40.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12891385 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:30.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13821905 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:13:50.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11580919 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:25.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11560414 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:56.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11552521 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:40.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626588 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:04.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11579514 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:26467025

  • This annotation was curated on 2020-03-26 10:16:14.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11548266 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:59.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11637997 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:24033266, PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:54.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11591249 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:35.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12888945 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:37.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14689950 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:49.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11348491 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:51.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11346956 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:26.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11577813 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:11.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11352140 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:41.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626595 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:23054246, PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:02.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11633650 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:18710658, PMID:25741868, PMID:26467025, PMID:27765764, PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:47.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13810066 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:23.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12883091 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:10.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11583204 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:02.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11525749 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:30.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11595636 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:19:13.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13805534 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:33.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11586419 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:20.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11347120 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:04.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10449750 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:24033266, PMID:25741868, PMID:26467025, PMID:28492532, PMID:8889592, PMID:8960785, PMID:9490296

  • This annotation was curated on 2020-03-26 10:16:45.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10449887 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: Familial hypobetalipoproteinemia
  • Original References(s): PMID:25741868, PMID:26467025, PMID:27765764, PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:59.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13626643 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:56.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11347605 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:16:37.0 by RGD . For more information contact us

    An association has been curated linking APOB and hypobetalipoproteinemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12882607 (Homo sapiens)
  • 10 RGD objects have been annotated to hypobetalipoproteinemia  (DOID:1390)
  • 47 papers in RGD have been used to annotate APOB
  • Curation Notes: ClinVar Annotator: match by term: HYPOBETALIPOPROTEINEMIA, FAMILIAL
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:18:17.0 by RGD . For more information contact us

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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.