Congenital nephrotic syndrome, Finnish type

Go to external page http://www.orpha.net/ORDO/Orphanet_839


A rare congenital nephrotic syndrome characterized by massive protein loss and marked edema manifesting <i>in utero</i> or during the first 3 months of life.

Synonyms:

Finnish congenital nephrosis

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=839
hasDbXref
  • MedDRA:10060740
  • OMIM:256300
  • UMLS:C0403399
  • MeSH:C535761
  • ICD-10:N04.8
has age of onset
  • http://www.orpha.net/ORDO/Orphanet_409944
  • http://www.orpha.net/ORDO/Orphanet_409943
  • http://www.orpha.net/ORDO/Orphanet_409945
has birth prevalence range
  • http://www.orpha.net/ORDO/Orphanet_409975
has inheritance
  • http://www.orpha.net/ORDO/Orphanet_409930
has point prevalence range
  • http://www.orpha.net/ORDO/Orphanet_409981
notation
  • ORPHA:839
part of
  • http://www.orpha.net/ORDO/Orphanet_564127
present in
  • http://www.orpha.net/ORDO/Orphanet_410065
  • http://www.orpha.net/ORDO/Orphanet_409991