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Summary Literature (0)
MIM:607855 - MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A

Xenbase Genes: lama2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011925 - congenital merosin-deficient muscular dystrophy 1A

Disease Ontology (DO):
DOID:0110636 - congenital merosin-deficient muscular dystrophy 1A