nephrotic syndrome type 1 (Q61913400)
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familial nephrotic syndrome characterized by prenatal onset of massive proteinuria followed by steroid resistant renal disease that has material basis in homozygous or compound heterozygous mutation in the NPHS1 gene on chromosome 19q13
- Finnish congenital nephrosis
- NPHS1
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | nephrotic syndrome type 1 |
familial nephrotic syndrome characterized by prenatal onset of massive proteinuria followed by steroid resistant renal disease that has material basis in homozygous or compound heterozygous mutation in the NPHS1 gene on chromosome 19q13 |
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