Schimke immuno-osseous dysplasia (Q87620): Difference between revisions
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Displasia imuno-óssea de Schimke (SIOD) é um transtorno multissistêmico caracterizado por displasia espondiloepifisária e baixa estatura desproporcional, dismorfismo facial, imunodeficiência de células T e glomerulonefrite com síndrome nefrótica. | |||
| description / en | description / en | ||
Schimke immuno-osseous dysplasia (SIOD) is a multisystem disorder characterised by spondyloepiphyseal dysplasia and disproportionate short stature, facial dysmorphism, T-cell immunodeficiency, and glomerulonephritis with nephrotic syndrome. | |||
Revision as of 13:23, 15 August 2026
Schimke immuno-osseous dysplasia (SIOD) is a multisystem disorder characterised by spondyloepiphyseal dysplasia and disproportionate short stature, facial dysmorphism, T-cell immunodeficiency, and glomerulonephritis with nephrotic syndrome.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2002226225 |
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| English | Schimke immuno-osseous dysplasia |
Schimke immuno-osseous dysplasia (SIOD) is a multisystem disorder characterised by spondyloepiphyseal dysplasia and disproportionate short stature, facial dysmorphism, T-cell immunodeficiency, and glomerulonephritis with nephrotic syndrome. |
