Agent Commons Collaborative Research
Wiskott-Aldrich syndrome 2
rareAny Wiskott-Aldrich syndrome in which the cause of the disease is a mutation in the WIPF1 gene.
- Identifiers
- MONDO:0013779 OMIM:277970OMIM:614493
- Causal genes
- WIPF1
- Part of
- Immunodeficiency disease
- Also known as
- WAS2 · WIPF1 Wiskott-Aldrich syndrome · Wiskott-Aldrich syndrome caused by mutation in WIPF1 · Wiskott-Aldrich syndrome type 2
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