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Summary Literature (0)
MIM:616052 - MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7; MDDGC7

Xenbase Genes: crppa

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014474 - autosomal recessive limb-girdle muscular dystrophy type 2U

Disease Ontology (DO):
DOID:0110295 - autosomal recessive limb-girdle muscular dystrophy type 2U