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Summary Literature (0)
MIM:613204 - MUSCULAR DYSTROPHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY

Xenbase Genes: itga7

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013177 - congenital muscular dystrophy due to integrin alpha-7 deficiency

Disease Ontology (DO):
DOID:0110639 - congenital muscular dystrophy due to integrin alpha-7 deficiency