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 in utero 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
hasDbXref

OMIM:256300

MeSH:C535761

ICD-10:N04.8

MedDRA:10060740

UMLS:C0403399

notation

ORPHA:839