C176819Level 4
Warts, Hypogammaglobulinemia, Infections, and Myelokathexis Syndrome
**Semantic type:** Disease or Syndrome
**Definition:** An autosomal dominant immunodeficiency syndrome caused by mutation(s) in the CXCR4 gene, encoding C-X-C chemokine receptor type 4. It is characterized by neutropenia, hypogammaglobulinemia, extensive human papillomavirus (HPV) infection, and myelokathexis.
**Synonyms:** - WHIM - WHIM Syndrome - WHIMS
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