(Q928424)

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
  • 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

Statements

Barth syndrome
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Identifiers

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