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Summary Literature (0)
MIM:608423 - MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 2; LGMDD2

Xenbase Genes: tnpo3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012034 - autosomal dominant limb-girdle muscular dystrophy type 1F

Disease Ontology (DO):
DOID:0110304 - autosomal dominant limb-girdle muscular dystrophy type 2