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Wiskott-Aldrich syndrome 2

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any Wiskott-Aldrich syndrome in which the cause of the disease is a mutation in the WIPF1 gene.
Uniprot Description An immunodeficiency disorder characterized by eczema, thrombocytopenia, recurrent infections, defective T-cell proliferation, and impaired natural killer cell function.
Mondo Term and Equivalent IDs
MONDO:0013779:  Wiskott-Aldrich syndrome 2
UMLS:C3281001: