Term Name:	autosomal recessive limb-girdle muscular dystrophy type 2M
Synonyms:	LGMD2M, MDDGC4, muscular dystrophy-dystroglycanopathy (limb-girdle) type C 4
Definition:	An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding fukutin (FKTN) on chromosome 9q31.
Ontology:	Human Disease [DOID:0110296]   ( DOID:0110296 )