Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Echinobase
Summary Literature (0)
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

Echinobase Genes : 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): muscular dystrophy-dystroglycanopathy (is_a)