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Summary Literature (0)
MIM:608099 - MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 3; LGMDR3

Xenbase Genes: sgca

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011968 - autosomal recessive limb-girdle muscular dystrophy type 2D

Disease Ontology (DO):
DOID:0110278 - autosomal recessive limb-girdle muscular dystrophy type 2D