WHIM syndrome (Q1258463)

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An immunodeficiency disease characterized by neutropenia, hypogammaglobulinemia, and extensive human papillomavirus (HPV) infection. It has material basis in heterozygous mutation in the CXCR4 gene on chromosome 2q22.
  • WHIMS
  • warts, hypogammaglobulinemia, infections, and myelokathexis
  • warts-hypogammaglobulinemia-infections-myelokathexis syndrome
  • WHIM SYNDROME; WHIMS
  • Warts-infections-leukopenia-myelokatexis syndrome
  • WHIM SYNDROME
  • Warts, Hypogammaglobulinemia, Infections, and Myelokathexis Syndrome
  • WILM
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English
WHIM syndrome
An immunodeficiency disease characterized by neutropenia, hypogammaglobulinemia, and extensive human papillomavirus (HPV) infection. It has material basis in heterozygous mutation in the CXCR4 gene on chromosome 2q22.
  • WHIMS
  • warts, hypogammaglobulinemia, infections, and myelokathexis
  • warts-hypogammaglobulinemia-infections-myelokathexis syndrome
  • WHIM SYNDROME; WHIMS
  • Warts-infections-leukopenia-myelokatexis syndrome
  • WHIM SYNDROME
  • Warts, Hypogammaglobulinemia, Infections, and Myelokathexis Syndrome
  • WILM

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