ORPHA:324294
T-cell immunodeficiency with epidermodysplasia verruciformis
Also called T-cell immunodeficiency due to RHOH deficiency
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Childhood
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:324294 is classified under "Immunological diseases" in the Orphanet nomenclature.