CLRN1, clarin 1, 7401

N. diseases: 77; N. variants: 26
Disease: Cataract ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0086543
Disease: Cataract
Cataract 		0.110 GeneticVariation disease BEFREE We have identified a consanguineous Lebanese family with two affected members displaying progressive hearing loss, RP and cataracts, therefore clinically diagnosed as USH type 3 (USH3). 22938382 2012
CUI: C0086543
Disease: Cataract
Cataract 		0.110 Biomarker disease HPO