DMD, dystrophin, 1756

N. diseases: 484; N. variants: 345
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 GeneticVariation disease BEFREE Giant dystrophin deletion associated with congenital cataract and mild muscular dystrophy. 9710043 1998