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Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Peroxisomal Disorders > Acatalasia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Peroxisomal Disorders > Acatalasia

Preferred term

Acatalasia  

Type

  • Topical Descriptor

Broader concept

Entry terms

  • Acatalasemia
  • Disease, Takahara
  • Disease, Takahara's
  • Takahara Disease
  • Takahara's Disease
  • Takaharas Disease

Scope note

  • A rare autosomal recessive disorder resulting from the absence of CATALASE activity. Though usually asymptomatic, a syndrome of oral ulcerations and gangrene may be present.

History note

  • 2000

In other languages

  • akatalasia

    Finnish

  • acatalasia
  • katalaasin puute
  • katalaasin puutos
  • morbus Takahara
  • Takahara
  • Takaharan sairaus
  • Takaharan tauti
  • Akatalasemi

    Swedish

URI

http://www.yso.fi/onto/mesh/D020642

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