CLRN1, clarin 1, 7401

N. diseases: 77; N. variants: 26
Disease: Congenital cataract ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0009691
Disease: Congenital cataract
Congenital cataract 		0.010 Biomarker disease BEFREE The phenotype is similar, but not identical to that of USH3 patients, as congenital cataract has not been reported for USH3. 20236115 2010