Pierson syndrome (Q104701)
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Pierson syndrome is a genetic disorder characterised by the association of congenital nephrotic syndrome with diffuse mesangial sclerosis and ocular anomalies with microcoria.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_555082533 |
||
| English | Pierson syndrome |
Pierson syndrome is a genetic disorder characterised by the association of congenital nephrotic syndrome with diffuse mesangial sclerosis and ocular anomalies with microcoria. |
Statements
CID11:ID_555082533
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