Rare Zebra

Rare disease search prototype built on Orphanet data

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ORPHA:906

Wiskott-Aldrich syndrome

Also called Eczema-thrombocytopenia-immunodeficiency syndrome, WAS

Body system
Skin diseases
Inheritance pattern
Autosomal dominant, Autosomal recessive, Not applicable, X-linked recessive
Typical age of onset
Infancy, Neonatal
Estimated prevalence
1-9 / 1 000 000 (Europe)
Rarity class
1-9 / 1 000 000

ORPHA:906 is classified under "Skin diseases" in the Orphanet nomenclature.

Common signs

  • Sinusitis
  • Otitis media
  • Chronic otitis media
  • Bruising susceptibility
  • Thrombocytopenia
  • Lymphopenia