Human genes for autosomal recessive limb-girdle muscular dystrophy type 2M
Autosomal recessive limb-girdle muscular dystrophy type 2M [DOID:0110296]
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.
Synonyms: autosomal recessive limb-girdle muscular dystrophy type 2M, autosomal recessive limbgirdle muscular dystrophy type 2M, DOID:0110296, LGMD2M, MDDGC4 ...