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Summary Literature (0)
MIM:613157 - MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3; MDDGC3

Xenbase Genes: pomgnt1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013161 - autosomal recessive limb-girdle muscular dystrophy type 2O

Disease Ontology (DO):
DOID:0110292 - autosomal recessive limb-girdle muscular dystrophy type 2O