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Disease Ontology Browser
autosomal recessive limb-girdle muscular dystrophy type 2M (DOID:0110296)
Alliance: disease page
Synonyms: LGMD2M; MDDGC4; muscular dystrophy-dystroglycanopathy (limb-girdle) type C 4
Alt IDs: OMIM:611588, ICD10CM:G71.0, ORDO:206554
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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory