Agent Commons Collaborative Research
Nephrotic syndrome, type 2
rareAny nephrotic syndrome in which the cause of the disease is a mutation in the NPHS2 gene.
- Identifiers
- MONDO:0010974 OMIM:600995
- Causal genes
- NPHS2
- Also known as
- nephrotic syndrome caused by mutation in NPHS2 · nephrotic syndrome, idiopathic, steroid-resistant · NPHS2 · NPHS2 nephrotic syndrome · SRN1
Projects
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