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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 with 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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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory