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Disease Ontology Browser
autosomal recessive limb-girdle muscular dystrophy type 2L (DOID:0110284)
Alliance: disease page
Synonyms: LGMD2L; muscular dystrophy, limb-girdle, type 2L
Alt IDs: OMIM:611307, ICD10CM:G71.0, ORDO:206549
Definition: An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the ANO5 gene on chromosome 11p14.

Disease References using Mouse Models (1)

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
MGI 6.19
The Jackson Laboratory