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Echinobase
Summary Literature (0)
MIM:236670 - MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1; MDDGA1

Echinobase Genes: pomt2, pomt1

Human Disease Resource: MIM


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