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Summary Literature (0)
MIM:601954 - MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 7; LGMDR7

Xenbase Genes: tcap

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011170 - autosomal recessive limb-girdle muscular dystrophy type 2G

Disease Ontology (DO):
DOID:0110281 - autosomal recessive limb-girdle muscular dystrophy type 2G