Pierson syndrome (Q104701): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed label, description and/or aliases in pt-br, en |
Changed an Item |
||
| Property / Canonical URI | |||
| Property / Canonical URI: https://id.who.int/icd/entity/555082533 / rank | |||
Normal rank | |||
Revision as of 10:34, 17 August 2026
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. |
