Orphanet: Wiskott Aldrich syndrome

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Wiskott-Aldrich syndrome

Disease definition

A primary immunodeficiency disease characterized by microthrombocytopenia, eczema, infections and an increased risk for autoimmune manifestations and malignancies.


Classification level: Disorder
  • Synonym(s):
    • Eczema-thrombocytopenia-immunodeficiency syndrome
    • WAS
  • Prevalence: 1-9 / 1 000 000
  • Inheritance: Autosomal dominant or Autosomal recessive or X-linked recessive or Not applicable 
  • Age of onset: Infancy, Neonatal
  • ICD-10: D82.0
  • OMIM: 301000  600903  614493
  • UMLS: C0043194
  • MeSH: D014923
  • GARD: 7895
  • MedDRA: 10047992
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