Category:Barth syndrome

**Barth syndrome**
	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
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Instance of	developmental defect during embryogenesis; rare disease; class of disease;
Subclass of	lipid metabolism disorder; 3-methylglutaconic aciduria; syndromic dyslipidemia; mitochondrial myopathy; 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;
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	Q928424;
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Media in category "Barth syndrome"

The following 2 files are in this category, out of 2 total.