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Disease Ontology Browser
autosomal recessive limb-girdle muscular dystrophy type 2G (DOID:0110281)
Alliance: disease page
Synonyms: LGMD2G; limb-girdle muscular dystrophy due to telethonin deficiency; muscular dystrophy, limb-girdle, type 2G
Alt IDs: OMIM:601954, ICD10CM:G71.0, ORDO:34514
Definition: An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in mutation in the gene encoding telethonin (TCAP).

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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05/10/2022
MGI 6.19 		The Jackson Laboratory