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DOID:0112374 - muscular dystrophy-dystroglycanopathy
Disease Ontology Definition:A congenital muscular dystrophy characterized by muscular dystrophy resulting from defective glycosylation of dystroglycan.
Synonyms: CMD due to dystroglycanopathy, congenital muscular dystrophy due to dystroglycanopathy, MDDG
Xenbase Genes
:
gmppb,
pomt1,
pomgnt1,
fkrp,
fktn,
pomgnt2,
pomk,
pomt2,
b4gat1,
rxylt1,
b3galnt2,
crppa,
large1
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)