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Summary Literature (0)
MIM:613156 - MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 2; MDDGB2

Xenbase Genes: pomt2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013160 - epithalamus ventricular layer
MONDO:0018277 - obsolete congenital muscular dystrophy with cerebellar involvement
MONDO:0018278 - congenital muscular dystrophy with intellectual disability

Disease Ontology (DO):
DOID:0112380 - muscular dystrophy-dystroglycanopathy type B2