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GENE - TERM ANNOTATION REPORT

22 Annotations Found.

An association has been curated linking GPI and congenital nonspherocytic hemolytic anemia 4 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151772157 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nonspherocytic hemolytic anemia 4  (DOID:0051005)
  • 17 papers in RGD have been used to annotate GPI
  • Curation Notes: ClinVar Annotator: match by term: ANEMIA, CONGENITAL, NONSPHEROCYTIC HEMOLYTIC, 4
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30337328 PMID:31133865


    • An association has been curated linking GPI and congenital nonspherocytic hemolytic anemia 4 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11544776|RGD:13437069|RGD:15111976|RGD:15114225|RGD:15150851|RGD:15166187|RGD:21406079|RGD:243057884|RGD:41405665 (Homo sapiens) & RGD:11544776|RGD:13437069|RGD:15111976|RGD:15114225|RGD:15150851|RGD:15166187|RGD:21406079|RGD:243057884|RGD:41405665 (Homo sapiens) & RGD:11544776|RGD:13437069|RGD:15111976|RGD:15114225|RGD:15150851|RGD:15166187|RGD:21406079|RGD:243057884|RGD:41405665 (Homo sapiens) & RGD:11544776|RGD:13437069|RGD:15111976|RGD:15114225|RGD:15150851|RGD:15166187|RGD:21406079|RGD:243057884|RGD:41405665 (Homo sapiens) & RGD:11544776|RGD:13437069|RGD:15111976|RGD:15114225|RGD:15150851|RGD:15166187|RGD:21406079|RGD:243057884|RGD:41405665 (Homo sapiens) & RGD:11544776|RGD:13437069|RGD:15111976|RGD:15114225|RGD:15150851|RGD:15166187|RGD:21406079|RGD:243057884|RGD:41405665 (Homo sapiens) & RGD:11544776|RGD:13437069|RGD:15111976|RGD:15114225|RGD:15150851|RGD:15166187|RGD:21406079|RGD:243057884|RGD:41405665 (Homo sapiens) & RGD:11544776|RGD:13437069|RGD:15111976|RGD:15114225|RGD:15150851|RGD:15166187|RGD:21406079|RGD:243057884|RGD:41405665 (Homo sapiens) & RGD:11544776|RGD:13437069|RGD:15111976|RGD:15114225|RGD:15150851|RGD:15166187|RGD:21406079|RGD:243057884|RGD:41405665 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nonspherocytic hemolytic anemia 4  (DOID:0051005)
  • 17 papers in RGD have been used to annotate GPI
  • Curation Notes: ClinVar Annotator: match by term: ANEMIA, CONGENITAL, NONSPHEROCYTIC HEMOLYTIC, 4 | ClinVar Annotator: match by term: GPI-related condition | ClinVar Annotator: match by term: Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking GPI and congenital nonspherocytic hemolytic anemia 4 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8563826 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nonspherocytic hemolytic anemia 4  (DOID:0051005)
  • 17 papers in RGD have been used to annotate GPI
  • Curation Notes: ClinVar Annotator: match by term: Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency
  • Original References(s): PMID:8499925


    • An association has been curated linking GPI and congenital nonspherocytic hemolytic anemia 4 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8599479 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nonspherocytic hemolytic anemia 4  (DOID:0051005)
  • 17 papers in RGD have been used to annotate GPI
  • Curation Notes: ClinVar Annotator: match by term: ANEMIA, CONGENITAL, NONSPHEROCYTIC HEMOLYTIC, 4
  • Original References(s): PMID:9856489


    • An association has been curated linking GPI and congenital nonspherocytic hemolytic anemia 4 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8599478 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nonspherocytic hemolytic anemia 4  (DOID:0051005)
  • 17 papers in RGD have been used to annotate GPI
  • Curation Notes: ClinVar Annotator: match by term: ANEMIA, CONGENITAL, NONSPHEROCYTIC HEMOLYTIC, 4
  • Original References(s): PMID:4076245 PMID:9856489


    • An association has been curated linking GPI and congenital nonspherocytic hemolytic anemia 4 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to congenital nonspherocytic hemolytic anemia 4  (DOID:0051005)
  • 17 papers in RGD have been used to annotate GPI


    • An association has been curated linking GPI and congenital nonspherocytic hemolytic anemia 4 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8599475 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nonspherocytic hemolytic anemia 4  (DOID:0051005)
  • 17 papers in RGD have been used to annotate GPI
  • Curation Notes: ClinVar Annotator: match by term: Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency
  • Original References(s): PMID:19064002 PMID:25741868 PMID:31133865 PMID:8499925


    • An association has been curated linking GPI and congenital nonspherocytic hemolytic anemia 4 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:21404584 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nonspherocytic hemolytic anemia 4  (DOID:0051005)
  • 17 papers in RGD have been used to annotate GPI
  • Curation Notes: ClinVar Annotator: match by term: Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency
  • Original References(s): PMID:32581362


    • An association has been curated linking GPI and congenital nonspherocytic hemolytic anemia 4 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151349692|RGD:151349958|RGD:152977976|RGD:152978096|RGD:329955167|RGD:401937190|RGD:402499174|RGD:402499495|RGD:402499505|RGD:402499515|RGD:407572994|RGD:41405313|RGD:41405450|RGD:598127928|RGD:598128011|RGD:598128084|RGD:598128099 (Homo sapiens) & RGD:151349692|RGD:151349958|RGD:152977976|RGD:152978096|RGD:329955167|RGD:401937190|RGD:402499174|RGD:402499495|RGD:402499505|RGD:402499515|RGD:407572994|RGD:41405313|RGD:41405450|RGD:598127928|RGD:598128011|RGD:598128084|RGD:598128099 (Homo sapiens) & RGD:151349692|RGD:151349958|RGD:152977976|RGD:152978096|RGD:329955167|RGD:401937190|RGD:402499174|RGD:402499495|RGD:402499505|RGD:402499515|RGD:407572994|RGD:41405313|RGD:41405450|RGD:598127928|RGD:598128011|RGD:598128084|RGD:598128099 (Homo sapiens) & RGD:151349692|RGD:151349958|RGD:152977976|RGD:152978096|RGD:329955167|RGD:401937190|RGD:402499174|RGD:402499495|RGD:402499505|RGD:402499515|RGD:407572994|RGD:41405313|RGD:41405450|RGD:598127928|RGD:598128011|RGD:598128084|RGD:598128099 (Homo sapiens) & RGD:151349692|RGD:151349958|RGD:152977976|RGD:152978096|RGD:329955167|RGD:401937190|RGD:402499174|RGD:402499495|RGD:402499505|RGD:402499515|RGD:407572994|RGD:41405313|RGD:41405450|RGD:598127928|RGD:598128011|RGD:598128084|RGD:598128099 (Homo sapiens) & RGD:151349692|RGD:151349958|RGD:152977976|RGD:152978096|RGD:329955167|RGD:401937190|RGD:402499174|RGD:402499495|RGD:402499505|RGD:402499515|RGD:407572994|RGD:41405313|RGD:41405450|RGD:598127928|RGD:598128011|RGD:598128084|RGD:598128099 (Homo sapiens) & RGD:151349692|RGD:151349958|RGD:152977976|RGD:152978096|RGD:329955167|RGD:401937190|RGD:402499174|RGD:402499495|RGD:402499505|RGD:402499515|RGD:407572994|RGD:41405313|RGD:41405450|RGD:598127928|RGD:598128011|RGD:598128084|RGD:598128099 (Homo sapiens) & RGD:151349692|RGD:151349958|RGD:152977976|RGD:152978096|RGD:329955167|RGD:401937190|RGD:402499174|RGD:402499495|RGD:402499505|RGD:402499515|RGD:407572994|RGD:41405313|RGD:41405450|RGD:598127928|RGD:598128011|RGD:598128084|RGD:598128099 (Homo sapiens) & RGD:151349692|RGD:151349958|RGD:152977976|RGD:152978096|RGD:329955167|RGD:401937190|RGD:402499174|RGD:402499495|RGD:402499505|RGD:402499515|RGD:407572994|RGD:41405313|RGD:41405450|RGD:598127928|RGD:598128011|RGD:598128084|RGD:598128099 (Homo sapiens) & RGD:151349692|RGD:151349958|RGD:152977976|RGD:152978096|RGD:329955167|RGD:401937190|RGD:402499174|RGD:402499495|RGD:402499505|RGD:402499515|RGD:407572994|RGD:41405313|RGD:41405450|RGD:598127928|RGD:598128011|RGD:598128084|RGD:598128099 (Homo sapiens) & RGD:151349692|RGD:151349958|RGD:152977976|RGD:152978096|RGD:329955167|RGD:401937190|RGD:402499174|RGD:402499495|RGD:402499505|RGD:402499515|RGD:407572994|RGD:41405313|RGD:41405450|RGD:598127928|RGD:598128011|RGD:598128084|RGD:598128099 (Homo sapiens) & RGD:151349692|RGD:151349958|RGD:152977976|RGD:152978096|RGD:329955167|RGD:401937190|RGD:402499174|RGD:402499495|RGD:402499505|RGD:402499515|RGD:407572994|RGD:41405313|RGD:41405450|RGD:598127928|RGD:598128011|RGD:598128084|RGD:598128099 (Homo sapiens) & RGD:151349692|RGD:151349958|RGD:152977976|RGD:152978096|RGD:329955167|RGD:401937190|RGD:402499174|RGD:402499495|RGD:402499505|RGD:402499515|RGD:407572994|RGD:41405313|RGD:41405450|RGD:598127928|RGD:598128011|RGD:598128084|RGD:598128099 (Homo sapiens) & RGD:151349692|RGD:151349958|RGD:152977976|RGD:152978096|RGD:329955167|RGD:401937190|RGD:402499174|RGD:402499495|RGD:402499505|RGD:402499515|RGD:407572994|RGD:41405313|RGD:41405450|RGD:598127928|RGD:598128011|RGD:598128084|RGD:598128099 (Homo sapiens) & RGD:151349692|RGD:151349958|RGD:152977976|RGD:152978096|RGD:329955167|RGD:401937190|RGD:402499174|RGD:402499495|RGD:402499505|RGD:402499515|RGD:407572994|RGD:41405313|RGD:41405450|RGD:598127928|RGD:598128011|RGD:598128084|RGD:598128099 (Homo sapiens) & RGD:151349692|RGD:151349958|RGD:152977976|RGD:152978096|RGD:329955167|RGD:401937190|RGD:402499174|RGD:402499495|RGD:402499505|RGD:402499515|RGD:407572994|RGD:41405313|RGD:41405450|RGD:598127928|RGD:598128011|RGD:598128084|RGD:598128099 (Homo sapiens) & RGD:151349692|RGD:151349958|RGD:152977976|RGD:152978096|RGD:329955167|RGD:401937190|RGD:402499174|RGD:402499495|RGD:402499505|RGD:402499515|RGD:407572994|RGD:41405313|RGD:41405450|RGD:598127928|RGD:598128011|RGD:598128084|RGD:598128099 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nonspherocytic hemolytic anemia 4  (DOID:0051005)
  • 17 papers in RGD have been used to annotate GPI
  • Curation Notes: ClinVar Annotator: match by term: ANEMIA, CONGENITAL, NONSPHEROCYTIC HEMOLYTIC, 4 | ClinVar Annotator: match by term: GPI-related condition | ClinVar Annotator: match by term: Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency


    • An association has been curated linking GPI and congenital nonspherocytic hemolytic anemia 4 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens) & RGD:126729883|RGD:126729888|RGD:126747028|RGD:127286873|RGD:150335220|RGD:150335222|RGD:150335332|RGD:150532064|RGD:151349579|RGD:153303291|RGD:156185493|RGD:156335814|RGD:156346866|RGD:243057689|RGD:243057690|RGD:243057691|RGD:243057692|RGD:243057693|RGD:243057881|RGD:243057883|RGD:243057885|RGD:243057887|RGD:243057889|RGD:243058329|RGD:401721176|RGD:401855520|RGD:404977342|RGD:404977345|RGD:404977347|RGD:404977350|RGD:404977352|RGD:404977842|RGD:404977844|RGD:405855365|RGD:405869417|RGD:597830493 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nonspherocytic hemolytic anemia 4  (DOID:0051005)
  • 17 papers in RGD have been used to annotate GPI
  • Curation Notes: ClinVar Annotator: match by term: ANEMIA, CONGENITAL, NONSPHEROCYTIC HEMOLYTIC, 4 | ClinVar Annotator: match by term: GPI-related condition | ClinVar Annotator: match by term: Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency
  • Original References(s): PMID:25741868


    • An association has been curated linking GPI and congenital nonspherocytic hemolytic anemia 4 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127260763|RGD:15098856|RGD:15170029|RGD:401928675|RGD:41405733|RGD:597915886 (Homo sapiens) & RGD:127260763|RGD:15098856|RGD:15170029|RGD:401928675|RGD:41405733|RGD:597915886 (Homo sapiens) & RGD:127260763|RGD:15098856|RGD:15170029|RGD:401928675|RGD:41405733|RGD:597915886 (Homo sapiens) & RGD:127260763|RGD:15098856|RGD:15170029|RGD:401928675|RGD:41405733|RGD:597915886 (Homo sapiens) & RGD:127260763|RGD:15098856|RGD:15170029|RGD:401928675|RGD:41405733|RGD:597915886 (Homo sapiens) & RGD:127260763|RGD:15098856|RGD:15170029|RGD:401928675|RGD:41405733|RGD:597915886 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nonspherocytic hemolytic anemia 4  (DOID:0051005)
  • 17 papers in RGD have been used to annotate GPI
  • Curation Notes: ClinVar Annotator: match by term: ANEMIA, CONGENITAL, NONSPHEROCYTIC HEMOLYTIC, 4 | ClinVar Annotator: match by term: GPI-related condition | ClinVar Annotator: match by term: Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking GPI and congenital nonspherocytic hemolytic anemia 4 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13532195 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nonspherocytic hemolytic anemia 4  (DOID:0051005)
  • 17 papers in RGD have been used to annotate GPI
  • Curation Notes: ClinVar Annotator: match by term: Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency
  • Original References(s): PMID:24033266 PMID:25741868


    • An association has been curated linking GPI and congenital nonspherocytic hemolytic anemia 4 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150544403 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nonspherocytic hemolytic anemia 4  (DOID:0051005)
  • 17 papers in RGD have been used to annotate GPI
  • Curation Notes: ClinVar Annotator: match by term: Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency
  • Original References(s): PMID:10916680 PMID:25741868 PMID:27519939 PMID:28492532


    • An association has been curated linking GPI and congenital nonspherocytic hemolytic anemia 4 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8599474 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nonspherocytic hemolytic anemia 4  (DOID:0051005)
  • 17 papers in RGD have been used to annotate GPI
  • Curation Notes: ClinVar Annotator: match by term: Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency
  • Original References(s): PMID:25741868 PMID:8499925


    • An association has been curated linking GPI and congenital nonspherocytic hemolytic anemia 4 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8599476 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nonspherocytic hemolytic anemia 4  (DOID:0051005)
  • 17 papers in RGD have been used to annotate GPI
  • Curation Notes: ClinVar Annotator: match by term: Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency
  • Original References(s): PMID:26509025 PMID:28492532 PMID:30585945 PMID:8822954 PMID:9616041


    • An association has been curated linking GPI and congenital nonspherocytic hemolytic anemia 4 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:153302426 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nonspherocytic hemolytic anemia 4  (DOID:0051005)
  • 17 papers in RGD have been used to annotate GPI
  • Curation Notes: ClinVar Annotator: match by term: Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency
  • Original References(s): PMID:10916680 PMID:25741868


    • An association has been curated linking GPI and congenital nonspherocytic hemolytic anemia 4 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:153302425 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nonspherocytic hemolytic anemia 4  (DOID:0051005)
  • 17 papers in RGD have been used to annotate GPI
  • Curation Notes: ClinVar Annotator: match by term: Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency
  • Original References(s): PMID:10916680 PMID:25741868 PMID:8822952


    • An association has been curated linking GPI and congenital nonspherocytic hemolytic anemia 4 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12896846 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nonspherocytic hemolytic anemia 4  (DOID:0051005)
  • 17 papers in RGD have been used to annotate GPI
  • Curation Notes: ClinVar Annotator: match by term: GPI-related condition
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


    • An association has been curated linking GPI and congenital nonspherocytic hemolytic anemia 4 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8599477 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nonspherocytic hemolytic anemia 4  (DOID:0051005)
  • 17 papers in RGD have been used to annotate GPI
  • Curation Notes: ClinVar Annotator: match by term: Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency
  • Original References(s): PMID:25741868 PMID:28492532 PMID:7989588 PMID:8822954 PMID:9616041


    • An association has been curated linking GPI and congenital nonspherocytic hemolytic anemia 4 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152978027 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nonspherocytic hemolytic anemia 4  (DOID:0051005)
  • 17 papers in RGD have been used to annotate GPI
  • Curation Notes: ClinVar Annotator: match by term: Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency
  • Original References(s): PMID:19064002 PMID:28492532 PMID:7989588 PMID:9266190


    • An association has been curated linking GPI and congenital nonspherocytic hemolytic anemia 4 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8599480|RGD:8599481|RGD:8599482 (Homo sapiens) & RGD:8599480|RGD:8599481|RGD:8599482 (Homo sapiens) & RGD:8599480|RGD:8599481|RGD:8599482 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nonspherocytic hemolytic anemia 4  (DOID:0051005)
  • 17 papers in RGD have been used to annotate GPI
  • Curation Notes: ClinVar Annotator: match by term: Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency
  • Original References(s): PMID:8822954


    • An association has been curated linking GPI and congenital nonspherocytic hemolytic anemia 4 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150542414 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nonspherocytic hemolytic anemia 4  (DOID:0051005)
  • 17 papers in RGD have been used to annotate GPI
  • Curation Notes: ClinVar Annotator: match by term: Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency
  • Original References(s): PMID:17041899 PMID:25741868 PMID:27427187 PMID:28492532


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