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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: OMIM


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