|
DOID:0112375 - muscular dystrophy-dystroglycanopathy type B
Disease Ontology Definition:A muscular dystrophy-dystroglycanopathy characterized by early onset of muscle weakness, intellectual disability in most cases, and variable presence of mild brain anomalies.
Synonyms: MDDGB,
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):
muscular dystrophy-dystroglycanopathy (is_a)