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Disease association ontology term - MONDO:0009192 - Wolcott-Rallison syndrome

Term summary

ID
MONDO:0009192
Name
Wolcott-Rallison syndrome
Ontology or CV name
Disease association
Definition
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.

Parents

Annotation

Disease association

MONDO:0009192 - Wolcott-Rallison syndrome

References:

Genes: