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Congenital nephrotic syndrome, Finnish type

^ http://www.orpha.net/ORDO/Orphanet_839


Congenital nephrotic syndrome, Finnish type is characterised by protein loss beginning during foetal life.

Synonyms: Finnish congenital nephrosis

Term info

database cross reference
  • OMIM:256300 (E (exact mapping (the terms and the concepts are equivalent)))
  • MeSH:C535761 (E (exact mapping (the terms and the concepts are equivalent)))
  • ICD-10:N04.8 (NTBT (narrower term maps to a broader term))
  • UMLS:C0403399 (E (exact mapping (the terms and the concepts are equivalent)))
  • MedDRA:10060740 (E (exact mapping (the terms and the concepts are equivalent)))
  • ICD-10:N04.8 (Attributed)
hasDbXref

OMIM:256300, MeSH:C535761, ICD-10:N04.8, MedDRA:10060740, UMLS:C0403399

notation

ORPHA:839