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Summary Literature (0)
MIM:613151 - MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 3; MDDGB3

Xenbase Genes: pomgnt1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013155 - muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B3
MONDO:0018277 - obsolete congenital muscular dystrophy with cerebellar involvement

Disease Ontology (DO):
DOID:0112378 - muscular dystrophy-dystroglycanopathy type B3