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Echinobase
Summary Literature (0)
MIM:614643 - MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7

Echinobase Genes: crppa

Human Disease Resource: MIM


Disease Ontology (DO):
DOID:0050588 - muscular dystrophy-dystroglycanopathy type B1
DOID:0111234 - congenital muscular dystrophy-dystroglycanopathy A7