Skip to main

Medical Subject Headings (thesaurus)

Search from vocabulary

mapear
anotar
descargar

Concept information

Skin and Connective Tissue Diseases > Connective Tissue Diseases > Collagen Diseases > Nephritis, Hereditary
Urogenital Diseases > Female Urogenital Diseases and Pregnancy Complications > Female Urogenital Diseases > Urogenital Abnormalities > Nephritis, Hereditary
Urogenital Diseases > Male Urogenital Diseases > Urogenital Abnormalities > Nephritis, Hereditary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Urogenital Abnormalities > Nephritis, Hereditary
... > Urogenital Diseases > Female Urogenital Diseases and Pregnancy Complications > Female Urogenital Diseases > Urologic Diseases > Kidney Diseases > Nephritis > Nephritis, Hereditary
... > Urogenital Diseases > Male Urogenital Diseases > Urologic Diseases > Kidney Diseases > Nephritis > Nephritis, Hereditary

Término preferido

Nephritis, Hereditary  

Notice: Undefined index: in /var/www/html/model/Concept.php on line 545

Tipo

  • mesh:Descriptor

Definición

  • A group of inherited conditions characterized initially by HEMATURIA and slowly progressing to RENAL INSUFFICIENCY. The most common form is the Alport syndrome (hereditary nephritis with HEARING LOSS) which is caused by mutations in genes for TYPE IV COLLAGEN and defective GLOMERULAR BASEMENT MEMBRANE.

Concepto genérico

Etiquetas alternativas

  • Hereditary Interstitial Pyelonephritis
  • Hereditary Nephritis
  • Nephritis, Familial

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-M83JCS52-X

Descargue este concepto:

RDF/XML TURTLE JSON-LD Creado 1/1/99, última modificación 30/6/21