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Disease Ontology Browser
autosomal dominant limb-girdle muscular dystrophy type 1 (DOID:0110305)
Alliance: disease page
Synonyms: autosomal dominant limb-girdle muscular dystrophy type 1E; LGMD1D; muscular dystrophy limb-girdle type 1D; muscular dystrophy limb-girdle type 1E
Alt IDs: OMIM:603511, ICD10CM:G71.0, ORDO:34517
Definition: An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in heterozygous mutation in the DNAJB6 gene on chromosome 7q36.

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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11/05/2024
MGI 6.24 		The Jackson Laboratory