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

Término preferido

Polycystic Kidney, Autosomal Dominant  

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Tipo

  • mesh:Descriptor

Definición

  • Kidney disorders with autosomal dominant inheritance and characterized by multiple CYSTS in both KIDNEYS with progressive deterioration of renal function. Type 2 ADPKD is linked to gene mutation at the PKD2 locus on the long arm of CHROMOSOME 4. Type 1 ADPKD is linked to gene mutation at the PKD1 locus on the short arm of CHROMOSOME 16.

Concepto genérico

Etiquetas alternativas

  • ADPKD
  • Adult Polycystic Kidney Disease
  • Autosomal Dominant Polycystic Kidney
  • Kidney, Polycystic, Autosomal Dominant
  • Polycystic Kidney Disease, Adult
  • Polycystic Kidney Disease, Autosomal Dominant

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-M2FJ609G-1

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