Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 92211
Gene Symbol: CDHR1
CDHR1
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		0.180 GeneticVariation CLINVAR Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy. 30718709

2019
Entrez Id: 92211
Gene Symbol: CDHR1
CDHR1
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		0.180 CausalMutation CLINVAR Biallelic mutation of protocadherin-21 (PCDH21) causes retinal degeneration in humans. 20087419

2010