ORPHA:51636
WHIM syndrome
Also called WILM, Warts-hypogammaglobulinemia-infections-myelokathexis syndrome, Warts-infections-leukopenia-myelokatexis syndrome
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal dominant, Autosomal recessive, Not applicable
- Typical age of onset
- Adolescent, Adult, Childhood
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:51636 is classified under "Immunological diseases" in the Orphanet nomenclature.
Common signs
- Decreased total neutrophil count
- Lymphopenia
- Abnormality of neutrophil morphology
- Bone marrow hypercellularity
- Myelokathexis
- Pneumonia