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Wiskott-Aldrich syndrome
rareWiskott-Aldrich syndrome (WAS) is a primary immunodeficiency disease characterized by microthrombocytopenia, eczema, infections and an increased risk for autoimmune manifestations and malignancies.
- Identifiers
- MONDO:0010518 OMIM:301000Orphanet:906
- Causal genes
- WAS
- Part of
- X-linked diseaseCombined immunodeficiencyHereditary neoplastic syndromeInherited blood coagulation disorder
- Also known as
- eczema thrombocytopenia immunodeficiency syndrome · eczema-thrombocytopenia-immunodeficiency syndrome · Imd 2 · immunodeficiency 2 · WAS
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