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... > Urogenital Diseases > Female Urogenital Diseases and Pregnancy Complications > Female Urogenital Diseases > Urologic Diseases > Kidney Diseases > Kidney Diseases, Cystic > Polycystic Kidney Diseases > Polycystic Kidney, Autosomal Recessive
... > Urogenital Diseases > Male Urogenital Diseases > Urologic Diseases > Kidney Diseases > Kidney Diseases, Cystic > Polycystic Kidney Diseases > Polycystic Kidney, Autosomal Recessive
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Ciliopathies > Polycystic Kidney Diseases > Polycystic Kidney, Autosomal Recessive
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Abnormalities, Multiple > Ciliopathies > Polycystic Kidney Diseases > Polycystic Kidney, Autosomal Recessive

Término preferido

Polycystic Kidney, Autosomal Recessive  

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Tipo

  • mesh:Descriptor

Definición

  • 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.

Concepto genérico

Etiquetas alternativas

  • 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

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-NCXL6VTB-9

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RDF/XML TURTLE JSON-LD Creado 30/5/91, última modificación 30/6/21