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autosomal recessive limb-girdle muscular dystrophy type 2W (DOID:0110288)
Alliance: disease page
Synonyms: LGMD2W; muscular dystrophy, limb-girdle, type 2W
Alt IDs: OMIM:616827, ORDO:466801
Definition: An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in compound heterozygous mutation in the LIM zinc finger domain containing 2 gene (LIMS2) on chromosome 2q14.


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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last database update
05/10/2022
MGI 6.19
The Jackson Laboratory