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Disease association ontology term - MONDO:0013779 - Wiskott-Aldrich syndrome 2

Term summary

ID
MONDO:0013779
Name
Wiskott-Aldrich syndrome 2
Ontology or CV name
Disease association
Definition
Any Wiskott-Aldrich syndrome in which the cause of the disease is a mutation in the WIPF1 gene.

Parents

Annotation

Disease association

MONDO:0013779 - Wiskott-Aldrich syndrome 2

References:

Genes: