CLRN1, clarin 1, 7401

N. diseases: 77; N. variants: 26
Disease: Unspecified visual loss ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3665346
Disease: Unspecified visual loss
Unspecified visual loss 		0.110 GeneticVariation phenotype BEFREE Usher syndrome type III (USH3) characterized by progressive loss of vision and hearing is caused by mutations in the clarin-1 gene (CLRN1). 29044151 2017
CUI: C3665346
Disease: Unspecified visual loss
Unspecified visual loss 		0.110 Biomarker phenotype HPO