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Disease Ontology Browser
autosomal recessive limb-girdle muscular dystrophy type 2F (DOID:0110280)
Alliance: disease page
Synonyms: delta-sarcoglycanopathy; LGMD2F; limb-girdle muscular dystrophy due to delta-sarcoglycan deficiency
Alt IDs: OMIM:601287, ICD10CM:G71.0, ORDO:219
Definition: An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in mutation in the sarcoglycan-delta gene (SGCD).

Disease References using Mouse Models (5)

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