Wolcott-Rallison syndrome (Q8029730)
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Wolcott-Rallison syndrome (WRS) is a very rare genetic disease, characterized by permanent neonatal diabetes mellitus (PNDM) with multiple epiphyseal dysplasia and other clinical manifestations, including recurrent episodes of acute liver failure
- Epiphyseal dysplasia multiple with early-onset diabetes mellitus
- WRS
- Med-Iddm Syndrome
- Early-onset diabetes mellitus with multiple epiphyseal dysplasia
- Iddm-Med Syndrome
- Wolcott-Rallison Syndrome
- Wolcott Rallison syndrome
- EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Wolcott-Rallison syndrome |
Wolcott-Rallison syndrome (WRS) is a very rare genetic disease, characterized by permanent neonatal diabetes mellitus (PNDM) with multiple epiphyseal dysplasia and other clinical manifestations, including recurrent episodes of acute liver failure |
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C131007
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Wolcott–Rallison syndrome
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Wikipedia(4 entries)
- arwiki متلازمة والكوت راليسون
- enwiki Wolcott–Rallison syndrome
- fiwiki Wolcott–Rallisonin oireyhtymä
- itwiki Sindrome di Wolcott-Rallison
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Multilingual sites(1 entry)
- commonswiki Category:Wolcott–Rallison syndrome