BabelNet

bn:05504712n

Noun Named Entity

autosomal recessive limb-girdle muscular dystrophy type 2M LGMD2M MDDGC4 Muscular Dystrophy, Limb-Girdle, Type 2M MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4

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 Wikidata

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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 Wikidata

IS A

rare disease

GENETIC ASSOCIATION

fukutin

HEALTH SPECIALTY

neurology

Wikidata

autosomal recessive limb-girdle muscular dystrophy type 2M

Wikidata Alias

LGMD2M, MDDGC4, Muscular Dystrophy, Limb-Girdle, Type 2M, MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4, MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4; MDDGC4, muscular dystrophy-dystroglycanopathy (limb-girdle) type C 4