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
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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
  • 3-methylglutaconicaciduria type 2
  • 3-methylglutaconicaciduria type II
  • MGA Type 2
  • MGA type II

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