Wolcott-Rallison syndrome
(Q8029730)
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
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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Wolcott-Rallison syndrome
other details
| aliases |
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 |
| description | 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 |
External Links
| (P486) |
C536739
C536739 |
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226980
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H00766
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DOID:0090060
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1667
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C0432217
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E13
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5589
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MONDO_0009192
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| (P6366) |
2777254461
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| (P11143) |
Wolcott–Rallison syndrome
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| (P11430) |
DI-01149
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