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Summary Literature (0)
MIM:611588 - MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4; MDDGC4

Xenbase Genes: fktn

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012699 - autosomal recessive limb-girdle muscular dystrophy type 2M

Disease Ontology (DO):
DOID:0110296 - autosomal recessive limb-girdle muscular dystrophy type 2M