Autosomal dominant polycystic kidney disease

Go to external page http://www.orpha.net/ORDO/Orphanet_730


A rare, genetic, renal tubular disease characterized by progressive outgrowths of fluid-filled cysts from the renal epithelium, which can manifest with hematuria, urinary tract infections, hypertension, and abdominal or flank pain. The slowly progressive loss of kidney function may evolve to end stage kidney disease (ESKD).

Synonyms:

ADPKD

This is just here as a test because I lose it

Term information

database cross reference
expertlink
  • https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=730
hasDbXref
  • ICD-11:GB81
  • ICD-10:Q61.2
  • OMIM:173900
  • OMIM:613095
  • OMIM:600666
has age of onset
  • http://www.orpha.net/ORDO/Orphanet_409947
  • http://www.orpha.net/ORDO/Orphanet_409948
  • http://www.orpha.net/ORDO/Orphanet_409946
has inheritance
  • http://www.orpha.net/ORDO/Orphanet_409929
has point prevalence range
  • http://www.orpha.net/ORDO/Orphanet_409975
notation
  • ORPHA:730
part of
  • http://www.orpha.net/ORDO/Orphanet_156162
  • http://www.orpha.net/ORDO/Orphanet_400003
  • http://www.orpha.net/ORDO/Orphanet_93587
  • http://www.orpha.net/ORDO/Orphanet_399824
  • http://www.orpha.net/ORDO/Orphanet_506213
present in
  • http://www.orpha.net/ORDO/Orphanet_409984