Human genes for Barth syndrome
Barth syndrome [DOID:0050476]
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.
Synonyms: Barth syndrome, Barth disease, Barth disorder, Barth syndromes, DOID:0050476 ...
Linkouts: OMIM