Pierson syndrome (Q104701): Difference between revisions
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A síndrome de Pierson é uma doença genética caracterizada pela associação de síndrome nefrótica congênita com esclerose mesangial difusa e anomalias oculares com microcoria. | |||
| description / en | description / en | ||
Pierson syndrome is a genetic disorder characterised by the association of congenital nephrotic syndrome with diffuse mesangial sclerosis and ocular anomalies with microcoria. | |||
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 |
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| 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. |
