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Concept information

Preferred term

Albinism  

Type

  • Topical Descriptor

Note

  • general or unspecified; prefer specifics

Scope note

  • General term for a number of inherited defects of amino acid metabolism in which there is a deficiency or absence of pigment in the eyes, skin, or hair.

In other languages

  • Finnish

  • albiino
  • albiinous
  • albinism
  • albinismus
  • Chediak-Steinbrinck-Higashin oireyhtymä
  • Chediak-Steinbrinck-Higashin syndrooma
  • Chediak-Steinbrinck-Higashis syndrom
  • Cross syndrom
  • Crossin oireyhtymä
  • Crossin syndrooma
  • Hermansky-Pudlakin oireyhtymä
  • Hermansky-Pudlakin syndrooma
  • Hermansky-Pudlaks syndrom
  • syndroma Chediak-Steinbrinck-Higashi
  • syndroma Cross
  • syndroma Hermansky-Pudlak
  • syndroma Waardenburg
  • Waardenburg syndrom
  • Waardenburgin oireyhtymä
  • Waardenburgin syndrooma
  • Swedish

URI

http://www.yso.fi/onto/mesh/D000417

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