Barth syndrome (Q928424)
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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
- 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
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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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Cardiolipin.svg
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C84585
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Barth syndrome
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Identifiers
Barth Syndrome
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Sitelinks
Wikipedia(16 entries)
- arwiki متلازمة بارث
- cawiki Síndrome de Barth
- dewiki Barth-Syndrom
- enwiki Barth syndrome
- eswiki Síndrome de Barth
- fiwiki Barthin oireyhtymä
- frwiki Syndrome de Barth
- hewiki סינדרום בארס
- itwiki Sindrome di Barth
- nlwiki Syndroom van Barth
- plwiki Zespół Bartha
- ruwiki Синдром Барта
- srwiki Бартов синдром
- trwiki Barth sendromu
- uzwiki Bart sindromi
- zhwiki 巴氏症候群
Wikibooks(0 entries)
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Wikiquote(0 entries)
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Wikiversity(0 entries)
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Wiktionary(0 entries)
Multilingual sites(1 entry)
- commonswiki Category:Barth syndrome