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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 disease,
developmental defect during embryogenesis
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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Barth sendromu (tr); Zespół Bartha (pl); Syndrome de Barth (fr); 巴氏症候群 (zh); Síndrome de Barth (es); Barth-en sindrome (eu); סינדרום בארס (he); Syndroom van Barth (nl); Синдром Барта (ru); Barth syndrome (rup); Barth-Syndrom (de); sindrome di Barth (it); Barth syndrome (en); síndrome de Barth (ca); Bart syndrom (cs); Бартов синдром (sr) 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 (en); genetycznie uwarunkowane, dziedziczone recesywnie, sprzężone z płcią, zaburzenie metabolizmu fosfolipidów. (pl); Krankheit (de) 3-methylglutaconicaciduria type 2, 3-methylglutaconicaciduria type II, MGA Type 2, MGA type II, Cardioskeletal Myopathy With Neutropenia and Abnormal Mitochondria, BARTH SYNDROME, Cardioskeletal myopathy-neutropenia syndrome, MGA2, 3-methylglutaconic aciduria type 2, X-linked cardioskeletal myopathy and neutropenia, 3-methylglutaconic aciduria type II, 3-Methylglutaconic Aciduria, Type 2, BARTH SYNDROME; BTHS, Mga, Type 2, TAZ defect, BTHS (en); kwasica 3-metyloglutakonowa typu II, acyduria 3-metyloglutakonowa typu II, kardiomiopatia sprzężona z chromosomem X, włóknienie sprężyste wsierdzia typu 2 (pl); Sindrome de Barth (es)

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