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GENE - TERM ANNOTATION REPORT

25 Annotations Found.

An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11545606|RGD:11548603|RGD:28890740|RGD:405726717 (Homo sapiens) & RGD:11545606|RGD:11548603|RGD:28890740|RGD:405726717 (Homo sapiens) & RGD:11545606|RGD:11548603|RGD:28890740|RGD:405726717 (Homo sapiens) & RGD:11545606|RGD:11548603|RGD:28890740|RGD:405726717 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:25741868


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8660663 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11531191 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:23666964 PMID:25741868 PMID:26467025 PMID:28492532 PMID:31527833


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11059916 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:17298551 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11059907 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:17376234 PMID:20484225 PMID:25741868 PMID:28492532


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12738930 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:22955521 PMID:22974104 PMID:24781757 PMID:25720320 PMID:25741868 PMID:28492532 PMID:29177515 PMID:29978154 PMID:30854332 PMID:30877234 PMID:31589614 PMID:31981491 PMID:32581362 PMID:33854214


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13622185 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:22974104 PMID:24781757 PMID:28492532


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10767148 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532 PMID:34014604


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11345790 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:11423010 PMID:21858060 PMID:22904323 PMID:25741868 PMID:28492532


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11059913 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532 PMID:28546994 PMID:30680959 PMID:31527833


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8697485 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:25741868 PMID:28492532 PMID:28724664 PMID:30201732 PMID:35059314


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26920863 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:25741868 PMID:28492532 PMID:28724664


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11586507 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:25363768 PMID:25741868 PMID:28492532 PMID:28714951


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11347915|RGD:11645876|RGD:13502152|RGD:13622246|RGD:13806778|RGD:15188512|RGD:28889267 (Homo sapiens) & RGD:11347915|RGD:11645876|RGD:13502152|RGD:13622246|RGD:13806778|RGD:15188512|RGD:28889267 (Homo sapiens) & RGD:11347915|RGD:11645876|RGD:13502152|RGD:13622246|RGD:13806778|RGD:15188512|RGD:28889267 (Homo sapiens) & RGD:11347915|RGD:11645876|RGD:13502152|RGD:13622246|RGD:13806778|RGD:15188512|RGD:28889267 (Homo sapiens) & RGD:11347915|RGD:11645876|RGD:13502152|RGD:13622246|RGD:13806778|RGD:15188512|RGD:28889267 (Homo sapiens) & RGD:11347915|RGD:11645876|RGD:13502152|RGD:13622246|RGD:13806778|RGD:15188512|RGD:28889267 (Homo sapiens) & RGD:11347915|RGD:11645876|RGD:13502152|RGD:13622246|RGD:13806778|RGD:15188512|RGD:28889267 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:28492532


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11059920|RGD:11091935|RGD:11350395|RGD:11531195|RGD:12738931|RGD:12880800|RGD:8657674|RGD:8660654|RGD:8660655|RGD:8660657|RGD:8660658|RGD:8660659|RGD:8660660|RGD:8660661|RGD:8660662 (Homo sapiens) & RGD:11059920|RGD:11091935|RGD:11350395|RGD:11531195|RGD:12738931|RGD:12880800|RGD:8657674|RGD:8660654|RGD:8660655|RGD:8660657|RGD:8660658|RGD:8660659|RGD:8660660|RGD:8660661|RGD:8660662 (Homo sapiens) & RGD:11059920|RGD:11091935|RGD:11350395|RGD:11531195|RGD:12738931|RGD:12880800|RGD:8657674|RGD:8660654|RGD:8660655|RGD:8660657|RGD:8660658|RGD:8660659|RGD:8660660|RGD:8660661|RGD:8660662 (Homo sapiens) & RGD:11059920|RGD:11091935|RGD:11350395|RGD:11531195|RGD:12738931|RGD:12880800|RGD:8657674|RGD:8660654|RGD:8660655|RGD:8660657|RGD:8660658|RGD:8660659|RGD:8660660|RGD:8660661|RGD:8660662 (Homo sapiens) & RGD:11059920|RGD:11091935|RGD:11350395|RGD:11531195|RGD:12738931|RGD:12880800|RGD:8657674|RGD:8660654|RGD:8660655|RGD:8660657|RGD:8660658|RGD:8660659|RGD:8660660|RGD:8660661|RGD:8660662 (Homo sapiens) & RGD:11059920|RGD:11091935|RGD:11350395|RGD:11531195|RGD:12738931|RGD:12880800|RGD:8657674|RGD:8660654|RGD:8660655|RGD:8660657|RGD:8660658|RGD:8660659|RGD:8660660|RGD:8660661|RGD:8660662 (Homo sapiens) & RGD:11059920|RGD:11091935|RGD:11350395|RGD:11531195|RGD:12738931|RGD:12880800|RGD:8657674|RGD:8660654|RGD:8660655|RGD:8660657|RGD:8660658|RGD:8660659|RGD:8660660|RGD:8660661|RGD:8660662 (Homo sapiens) & RGD:11059920|RGD:11091935|RGD:11350395|RGD:11531195|RGD:12738931|RGD:12880800|RGD:8657674|RGD:8660654|RGD:8660655|RGD:8660657|RGD:8660658|RGD:8660659|RGD:8660660|RGD:8660661|RGD:8660662 (Homo sapiens) & RGD:11059920|RGD:11091935|RGD:11350395|RGD:11531195|RGD:12738931|RGD:12880800|RGD:8657674|RGD:8660654|RGD:8660655|RGD:8660657|RGD:8660658|RGD:8660659|RGD:8660660|RGD:8660661|RGD:8660662 (Homo sapiens) & RGD:11059920|RGD:11091935|RGD:11350395|RGD:11531195|RGD:12738931|RGD:12880800|RGD:8657674|RGD:8660654|RGD:8660655|RGD:8660657|RGD:8660658|RGD:8660659|RGD:8660660|RGD:8660661|RGD:8660662 (Homo sapiens) & RGD:11059920|RGD:11091935|RGD:11350395|RGD:11531195|RGD:12738931|RGD:12880800|RGD:8657674|RGD:8660654|RGD:8660655|RGD:8660657|RGD:8660658|RGD:8660659|RGD:8660660|RGD:8660661|RGD:8660662 (Homo sapiens) & RGD:11059920|RGD:11091935|RGD:11350395|RGD:11531195|RGD:12738931|RGD:12880800|RGD:8657674|RGD:8660654|RGD:8660655|RGD:8660657|RGD:8660658|RGD:8660659|RGD:8660660|RGD:8660661|RGD:8660662 (Homo sapiens) & RGD:11059920|RGD:11091935|RGD:11350395|RGD:11531195|RGD:12738931|RGD:12880800|RGD:8657674|RGD:8660654|RGD:8660655|RGD:8660657|RGD:8660658|RGD:8660659|RGD:8660660|RGD:8660661|RGD:8660662 (Homo sapiens) & RGD:11059920|RGD:11091935|RGD:11350395|RGD:11531195|RGD:12738931|RGD:12880800|RGD:8657674|RGD:8660654|RGD:8660655|RGD:8660657|RGD:8660658|RGD:8660659|RGD:8660660|RGD:8660661|RGD:8660662 (Homo sapiens) & RGD:11059920|RGD:11091935|RGD:11350395|RGD:11531195|RGD:12738931|RGD:12880800|RGD:8657674|RGD:8660654|RGD:8660655|RGD:8660657|RGD:8660658|RGD:8660659|RGD:8660660|RGD:8660661|RGD:8660662 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13475500 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:25741868 PMID:26467025 PMID:32462735


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:25322763 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28384794 PMID:28492532


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12738935 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:25394176 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11346192 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Paraganglioma, familial malignant
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28384794 PMID:28492532 PMID:29978154


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11040030 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28384794 PMID:28492532 PMID:28546994 PMID:28798025 PMID:29978154 PMID:30775854 PMID:32570879


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11531187|RGD:11531190 (Homo sapiens) & RGD:11531187|RGD:11531190 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:23666964 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12885989|RGD:12889711|RGD:12890002 (Homo sapiens) & RGD:12885989|RGD:12889711|RGD:12890002 (Homo sapiens) & RGD:12885989|RGD:12889711|RGD:12890002 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11586046|RGD:11589314|RGD:11644612|RGD:11647969|RGD:12845936|RGD:28890734|RGD:28893911|RGD:28894196|RGD:28903832 (Homo sapiens) & RGD:11586046|RGD:11589314|RGD:11644612|RGD:11647969|RGD:12845936|RGD:28890734|RGD:28893911|RGD:28894196|RGD:28903832 (Homo sapiens) & RGD:11586046|RGD:11589314|RGD:11644612|RGD:11647969|RGD:12845936|RGD:28890734|RGD:28893911|RGD:28894196|RGD:28903832 (Homo sapiens) & RGD:11586046|RGD:11589314|RGD:11644612|RGD:11647969|RGD:12845936|RGD:28890734|RGD:28893911|RGD:28894196|RGD:28903832 (Homo sapiens) & RGD:11586046|RGD:11589314|RGD:11644612|RGD:11647969|RGD:12845936|RGD:28890734|RGD:28893911|RGD:28894196|RGD:28903832 (Homo sapiens) & RGD:11586046|RGD:11589314|RGD:11644612|RGD:11647969|RGD:12845936|RGD:28890734|RGD:28893911|RGD:28894196|RGD:28903832 (Homo sapiens) & RGD:11586046|RGD:11589314|RGD:11644612|RGD:11647969|RGD:12845936|RGD:28890734|RGD:28893911|RGD:28894196|RGD:28903832 (Homo sapiens) & RGD:11586046|RGD:11589314|RGD:11644612|RGD:11647969|RGD:12845936|RGD:28890734|RGD:28893911|RGD:28894196|RGD:28903832 (Homo sapiens) & RGD:11586046|RGD:11589314|RGD:11644612|RGD:11647969|RGD:12845936|RGD:28890734|RGD:28893911|RGD:28894196|RGD:28903832 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11549948|RGD:11585146 (Homo sapiens) & RGD:11549948|RGD:11585146 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:25741868 PMID:26467025


  • An association has been curated linking SDHA and paraganglioma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11059909|RGD:11059911|RGD:11059915|RGD:11059917|RGD:11059919|RGD:11348859|RGD:11584675|RGD:11588435|RGD:8660656|RGD:8696853|RGD:8697434 (Homo sapiens) & RGD:11059909|RGD:11059911|RGD:11059915|RGD:11059917|RGD:11059919|RGD:11348859|RGD:11584675|RGD:11588435|RGD:8660656|RGD:8696853|RGD:8697434 (Homo sapiens) & RGD:11059909|RGD:11059911|RGD:11059915|RGD:11059917|RGD:11059919|RGD:11348859|RGD:11584675|RGD:11588435|RGD:8660656|RGD:8696853|RGD:8697434 (Homo sapiens) & RGD:11059909|RGD:11059911|RGD:11059915|RGD:11059917|RGD:11059919|RGD:11348859|RGD:11584675|RGD:11588435|RGD:8660656|RGD:8696853|RGD:8697434 (Homo sapiens) & RGD:11059909|RGD:11059911|RGD:11059915|RGD:11059917|RGD:11059919|RGD:11348859|RGD:11584675|RGD:11588435|RGD:8660656|RGD:8696853|RGD:8697434 (Homo sapiens) & RGD:11059909|RGD:11059911|RGD:11059915|RGD:11059917|RGD:11059919|RGD:11348859|RGD:11584675|RGD:11588435|RGD:8660656|RGD:8696853|RGD:8697434 (Homo sapiens) & RGD:11059909|RGD:11059911|RGD:11059915|RGD:11059917|RGD:11059919|RGD:11348859|RGD:11584675|RGD:11588435|RGD:8660656|RGD:8696853|RGD:8697434 (Homo sapiens) & RGD:11059909|RGD:11059911|RGD:11059915|RGD:11059917|RGD:11059919|RGD:11348859|RGD:11584675|RGD:11588435|RGD:8660656|RGD:8696853|RGD:8697434 (Homo sapiens) & RGD:11059909|RGD:11059911|RGD:11059915|RGD:11059917|RGD:11059919|RGD:11348859|RGD:11584675|RGD:11588435|RGD:8660656|RGD:8696853|RGD:8697434 (Homo sapiens) & RGD:11059909|RGD:11059911|RGD:11059915|RGD:11059917|RGD:11059919|RGD:11348859|RGD:11584675|RGD:11588435|RGD:8660656|RGD:8696853|RGD:8697434 (Homo sapiens) & RGD:11059909|RGD:11059911|RGD:11059915|RGD:11059917|RGD:11059919|RGD:11348859|RGD:11584675|RGD:11588435|RGD:8660656|RGD:8696853|RGD:8697434 (Homo sapiens)
  • 53 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 13 papers in RGD have been used to annotate SDHA
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


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