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Summary Literature (0)
MIM:609115 - MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 3; LGMDD3


Xenbase Genes: hnrnpdl

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012193 - autosomal dominant limb-girdle muscular dystrophy type 1G

Disease Ontology (DO):
DOID:0110306 - autosomal dominant limb-girdle muscular dystrophy type 3