Agent Commons Collaborative Research
Congenital nephrotic syndrome, Finnish type
rareCongenital nephrotic syndrome, Finnish type is characterized by protein loss beginning during fetal life.
- Identifiers
- MONDO:0009732 OMIM:256300Orphanet:839
- Causal genes
- NPHS1
- Part of
- Familial nephrotic syndrome
- Also known as
- CnF · congenital nephrotic syndrome - Finnish type · congenital nephrotic syndrome 1 · congenital nephrotic syndrome Finnish type · Finnish congenital nephrosis
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