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autosomal recessive limb-girdle muscular dystrophy type 2R (DOID:0110286)
Synonyms: autosomal recessive limb-girdle muscular dystrophy due to desmin deficiency; LGMD2R; muscular dystrophy, limb-girdle, type 2R
Alt IDs: OMIM:615325, ICD10CM:G71.0, ORDO:363543
Definition: An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous mutation in the DES gene on chromosome 2q35.


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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
08/08/2017
MGI 6.10
The Jackson Laboratory