ORPHA:674762
Early-onset autoinflammatory syndrome due to A20 haploinsufficiency
Also called Early-onset AID due to HA20, Early-onset autoinflammatory disorder due to HA20, Early-onset autoinflammatory syndrome associated with TNFAIP3, HA20-related monogenic Behcet-like disease
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Not documented in Orphadata
- Estimated prevalence
- Not documented in Orphadata
- Rarity class
- Not documented in Orphadata
ORPHA:674762 is classified under "Immunological diseases" in the Orphanet nomenclature.