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Summary Literature (0)
DOID:0112376 - muscular dystrophy-dystroglycanopathy type B15

Disease Ontology Definition:A muscular dystrophy-dystroglycanopathy type B that has_material_basis_in homozygous or compound heterozygous mutation in the DPM3 gene on chromosome 1q22.

Synonyms: MDDGB15, congenital muscular dystrophy DPM3-related,

Xenbase Genes :



Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a)