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Summary Literature (0)
MIM:613150 - MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2; MDDGA2

Xenbase Genes: pomt2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000171 - respiration organ
MONDO:0013154 - muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2
MONDO:0018939 - muscle-eye-brain disease