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Concept information

Preferred term

Polycystic Kidney, Autosomal Recessive  

Type

  • Topical Descriptor

Entry terms

  • ARPKD
  • Autosomal Recessive Polycystic Kidney
  • Autosomal Recessive Polycystic Kidney Disease
  • Kidney, Polycystic, Autosomal Recessive
  • Polycystic Kidney and Hepatic Disease 1
  • Polycystic Kidney and Hepatic Disease 1 (Autosomal Recessive)
  • Polycystic Kidney Disease, Autosomal Recessive
  • Polycystic Kidney Disease, Infantile, Type 1
  • Polycystic Kidney Disease, Infantile, Type I

Scope note

  • A genetic disorder with autosomal recessive inheritance, characterized by multiple CYSTS in both KIDNEYS and associated LIVER lesions. Serious manifestations are usually present at BIRTH with high PERINATAL MORTALITY.

History note

  • 1992

In other languages

  • Finnish

  • autosomaalisesti resessiivisesti periytyvät monirakkulaiset
  • autosomaalisesti resessiivisesti periytyvät monirakkulamunuaiset
  • autosomaalisesti resessiivisesti periytyvät polykystiset munuaiset
  • infantiili munuaisten monirakkulatauti
  • lapsuustyyppinen munuaisten monirakkulatauti
  • morbus polycysticus renalis autosomaticus recessivus
  • morbus polycysticus renalis infantilis
  • Swedish

URI

http://www.yso.fi/onto/mesh/D017044

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