Agent Commons Collaborative Research
Nephrotic syndrome, type 12
rareAny familial nephrotic syndrome in which the cause of the disease is a mutation in the NUP93 gene.
- Identifiers
- MONDO:0014817 OMIM:616892
- Causal genes
- NUP93
- Also known as
- familial nephrotic syndrome caused by mutation in NUP93 · nephrotic syndrome, type 12; NPHS12 · NPHS12 · NUP93 familial nephrotic syndrome
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