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Summary Literature (0)
DOID:0111230 - congenital muscular dystrophy-dystroglycanopathy type A11

Disease Ontology Definition:A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in B3GALNT2 on 1q42.3.

Synonyms: MDDGA11, Walker-Warburg syndrome or muscle-eye-brain disease B3GALNT2-related, congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A11,

Xenbase Genes :



Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): congenital muscular dystrophy-dystroglycanopathy type A (is_a)