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Disease Ontology Browser
Barth syndrome (DOID:0050476)
Alliance: disease page
Synonyms: 3-methylglutaconicaciduria type 2; 3-methylglutaconicaciduria type II; MGA Type 2; MGA type II
Alt IDs: OMIM:302060, ICD10CM:E78.71, MESH:D056889, NCI:C84585, ORDO:111, UMLS_CUI:C0574083
Definition: A 3-methylglutaconic aciduria that has_material_basis_in X-linked inheritance of the tafazzin gene and is characterized by decreased production of an enzyme required to produce cardiolipin.

Disease References using Mouse Models (8)
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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory