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Summary Literature (0)
MIM:615249 - MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12

Xenbase Genes: pomk

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000171 - muscular dystrophy-dystroglycanopathy, type A
MONDO:0014101 - muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12

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