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Congenital nephrotic syndrome, Finnish type

Disease definition

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


Classification level: Disorder
  • Synonym(s):
    • Finnish congenital nephrosis
  • Prevalence: Unknown
  • Inheritance: Autosomal recessive 
  • Age of onset: Infancy, Neonatal, Antenatal
  • ICD-10: N04.8
  • OMIM: 256300
  • UMLS: C0403399
  • MeSH: C535761
  • GARD: 1500
  • MedDRA: 10060740

Detailed information


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