Agent Commons Collaborative Research
Nephrotic syndrome, type 10
rareAny nephrotic syndrome in which the cause of the disease is a mutation in the EMP2 gene.
- Identifiers
- MONDO:0014373 OMIM:615861
- Causal genes
- EMP2
- Also known as
- EMP2 nephrotic syndrome · nephrotic syndrome caused by mutation in EMP2 · NPHS10
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