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


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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/14/2017
MGI 6.08
The Jackson Laboratory