muscular dystrophy-dystroglycanopathy

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Echinobase

Summary

Literature (0)

DOID:0112374 - muscular dystrophy-dystroglycanopathy

Disease Ontology Definition:A congenital muscular dystrophy characterized by muscular dystrophy resulting from defective glycosylation of dystroglycan.

Synonyms: MDDG

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: b3galnt2, b4gat1, crppa, gmppb, rxylt1, pomgnt2

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): congenital muscular dystrophy (is_a)