RHAG, Rh associated glycoprotein, 6005

N. diseases: 41; N. variants: 13
Disease: Rh Deficiency Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0272052
Disease: Rh Deficiency Syndrome
Rh Deficiency Syndrome 		0.300 GermlineCausalMutation disease ORPHANET Rh50 glycoprotein gene and rhnull disease: a silent splice donor is trans to a Gly279-->Glu missense mutation in the conserved transmembrane segment. 9716608 1998
CUI: C0272052
Disease: Rh Deficiency Syndrome
Rh Deficiency Syndrome 		0.300 GermlineCausalMutation disease ORPHANET Candidate gene acting as a suppressor of the RH locus in most cases of Rh-deficiency. 8563755 1996