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congenital nephrotic syndrome, Finnish type

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description Congenital nephrotic syndrome, Finnish type is characterised by protein loss beginning during foetal life.
Uniprot Description A form of nephrotic syndrome, a renal disease clinically characterized by severe proteinuria, resulting in complications such as hypoalbuminemia, hyperlipidemia and edema. Kidney biopsies show non-specific histologic changes such as focal segmental glomerulosclerosis and diffuse mesangial proliferation. Some affected individuals have an inherited steroid-resistant form and progress to end-stage renal failure.
Mondo Term and Equivalent IDs
MONDO:0009732:  congenital nephrotic syndrome, Finnish type
GARD:0001500: 
NCIT:C122795: 
Orphanet:839: 
SCTID:197601003: 
UMLS:C0403399: