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Summary Literature (0)
MIM:606612 - MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 5; MDDGB5

Xenbase Genes: fkrp

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011688 - muscular dystrophy-dystroglycanopathy type B5
MONDO:0018277 - obsolete congenital muscular dystrophy with cerebellar involvement
MONDO:0018278 - congenital muscular dystrophy with intellectual disability
MONDO:0018279 - obsolete congenital muscular dystrophy without intellectual disability

Disease Ontology (DO):
DOID:0110635 - muscular dystrophy-dystroglycanopathy type B5