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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 {http://www.w3.org/2004/02/skos/core#exactMatch="exactMatch"}, NCI:C84585, UMLS_CUI:C0574083
Definition: A lipid metabolism disorder 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 (7)

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
05/26/2020
MGI 6.15
The Jackson Laboratory