WHIM syndrome 1

A congenital autosomal dominant immune deficiency characterized by abnormal retention of mature neutrophils in the bone marrow (myelokathexis) and occasional hypogammaglobulinemia, associated with an increased risk for bacterial infections and a susceptibility to human papillomavirus (HPV) induced lesions (cutaneous warts, genital dysplasia and invasive mucosal carcinoma).

Also known as: WHIM syndrome, WHIM Syndrome, WHIMS, WILM, Warts, hypogammaglobulinemia, infections, and myelokathexis syndrome, Warts-hypogammaglobulinemia-infections-myelokathexis syndrome, Warts-infections-leukopenia-myelokatexis syndrome, myelokathexis, isolated

4 clinical trials for this condition and its sub-types, 4 tagged with WHIM syndrome 1 itself.