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Summary Literature (0)
MIM:253280 - MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3

Xenbase Genes: pomgnt1, fkrp

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000171 - respiration organ
MONDO:0009667 - muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3
MONDO:0018939 - muscle-eye-brain disease

Disease Ontology (DO):
DOID:0050560 - Walker-Warburg syndrome