RHAG, Rh associated glycoprotein, 6005

N. diseases: 41; N. variants: 13
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic
0.110 GeneticVariation disease BEFREE Recently, overhydrated hereditary stomatocytosis (OHSt), a rare dominantly inherited hemolytic anemia, was found to be associated with a mutation (Phe65Ser or Ile61Arg) in RHAG. 22012326 2012
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic
0.110 Biomarker disease HPO