Wiskott-Aldrich Syndrome 2

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal recessive condition caused by mutation(s) in the WIPF1 gene, encoding WAS/WASL-interacting protein family member 1. It is characterized by recurrent infections, eczema, thrombocytopenia, and T-cell and NK-cell dysfunction.

**Synonyms:** - WAS2 - WIP Deficiency - WIP Deficiency - Wiskott-Aldrich Syndrome Interacting Protein Deficiency - Wiskott-Aldrich Syndrome Interacting Protein Deficiency