All diseases

OMIM ID
606612
OMIM term:
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5; MDDGB5
Alternative terms:
MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C
MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED
(∗) Location:
19q13.32  
(†) Associated OMIM genes:
FKRP  
(‡) Associated MGI genes:
Fkrp  

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* quick link - http://q.sanger.ac.uk/rzbfuyhl