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Summary Literature (0)
MIM:615041 - MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 10; MDDGA10

Xenbase Genes: rxylt1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000171 - respiration organ
MONDO:0014022 - muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10

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