autosomal dominant limb-girdle muscular dystrophy type 1H Disease Ontology Browser

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Disease Ontology Browser

autosomal dominant limb-girdle muscular dystrophy type 1H (DOID:0110303)
Alliance: disease page
Synonyms: LGMD1H; muscular dystrophy limb-girdle type 1H
Alt IDs: OMIM:613530, ICD10CM:G71.0, ORDO:238755
Definition: An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in variation in the region 3p25.1-p23.

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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