Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23268
Gene Symbol: DNMBP
DNMBP
CUI: C0266539
Disease: Congenital total cataract
Congenital total cataract 		0.300 GermlineCausalMutation ORPHANET Bi-allelic Loss-of-Function Variants in DNMBP Cause Infantile Cataracts. 30290152

2018