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
|Instance of|| disease,|
developmental defect during embryogenesis
|Subclass of|| lipid metabolism disorder,|
constitutional neutropenia with extra-hematopoietic manifestations,
disorder of phospholipids, sphingolipids and fatty acids biosynthesis with skeletal muscle predominant involvement,
mitochondrial disease with dilated cardiomyopathy,
X-linked recessive disease
Media in category "Barth syndrome"
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