Rheumatology · Rheumatology / Autoinflammatory disease
Behçet-like haploinsufficiency of A20 syndrome
also: HA20
Early-onset Behçet-like autoinflammatory disease.
- Specialty
- Rheumatology
- Subspecialty
- Rheumatology / Autoinflammatory disease
- Sex & age distribution
- Male: affected; Female: affected equally; Children: yes
- Gene(s) involved
- TNFAIP3
- Alternative names & eponyms
- HA20
Etiology & mechanism
TNFAIP3 haploinsufficiency.
Gene(s) involved (1)
Symptoms & signs (5)
In plain terms, someone with Behçet-like haploinsufficiency of A20 syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
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Shares symptoms with
4 shared
Haploinsufficiency of A20 syndrome
arthritis, fever, genital ulcers, oral ulcers
2 shared
Antisynthetase syndrome
arthritis, fever
2 shared
Behçet syndrome
arthritis, genital ulcers
2 shared
Kostmann syndrome
fever, oral ulcers
2 shared
Stevens–Johnson syndrome
fever, oral ulcers
1 shared
Acquired immunodeficiency syndrome
fever
1 shared
Acute chest syndrome
fever
1 shared
Boerhaave syndrome
fever
1 shared
Caplan syndrome
arthritis
1 shared
Castleman syndrome
fever
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