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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, 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 (6)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.11
The Jackson Laboratory