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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
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"
This category contains only the following file.