RPGRIP1, RPGR interacting protein 1, 57096

N. diseases: 121; N. variants: 36
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0271388
Disease: Pendular Nystagmus
Pendular Nystagmus
0.400 Biomarker disease CTD_human Null RPGRIP1 alleles in patients with Leber congenital amaurosis. 11283794 2001
CUI: C0271388
Disease: Pendular Nystagmus
Pendular Nystagmus
0.400 GeneticVariation disease CLINVAR
CUI: C0271388
Disease: Pendular Nystagmus
Pendular Nystagmus
0.400 Biomarker disease HPO