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 |
(P492) |
226980
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(P665) |
H00766
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(P699) |
DOID:0090060
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(P1550) |
1667
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(P2892) |
C0432217
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(P4229) |
E13
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(P4317) |
5589
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(P5270) |
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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