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

Echinobase Genes: rxylt1

Human Disease Resource: MIM


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