nephrotic syndrome type 5 (Q61913388)
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familial nephrotic syndrome characterized by prenatal or neonatal onset of progressive renal failure with proteinurea and edema that has material basis in homozygous or compound heterozygous mutation in the LAMB2 gene on chromosome 3p
- nephrotic syndrome type 5, with or without ocular abnormalities
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | nephrotic syndrome type 5 |
familial nephrotic syndrome characterized by prenatal or neonatal onset of progressive renal failure with proteinurea and edema that has material basis in homozygous or compound heterozygous mutation in the LAMB2 gene on chromosome 3p |
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