Home Page
References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 16-09-2015
Symbol NPHP13
Location 4p14
Name nephronophthisis 13
Corresponding gene WDR19
Main clinical features
  • nephronophthisis, with mild proteinuria and a glomerular filtration rate at the lower limit of normal, or no symptom
  • in any cases, dilatation of the intrahepatic bile ducts
  • Genetic determination autosomal recessive
    Function/system disorder kidney and urinary tract
    Type disease
    Remark(s)