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)
MIM:615181 - MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11

Echinobase Genes: b3galnt2

Human Disease Resource: MIM


Disease Ontology (DO):
DOID:0050588 - muscular dystrophy-dystroglycanopathy type B1
DOID:0111230 - congenital muscular dystrophy-dystroglycanopathy type A11