Reactive arthritis

General Information (adopted from Orphanet):

Synonyms, Signs: Fiessinger-Leroy-Reiter syndrome
Venereal arthritis
Reiter syndrome
Polyarteritis enterica
Arthritis urethritica
Fiessinger-Leroy disease
Number of Symptoms 27
OrphanetNr: 29207
OMIM Id:
ICD-10: M02.8
UMLs: C0035012
C0085435
MeSH: D016918
MedDRA: 10003267
10038294
Snomed: 129133005
236690002
239783001
67224007

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Not applicable
[Orphanet]
Age of onset: All ages
[Orphanet]

Disease classification (adopted from Orphanet):

Parent Diseases: Rare rheumatologic disease
 -Rare systemic or rheumatologic disease

Symptom Information: Sort by abundance 

1
 (HPO:0000010) Recurrent urinary tract infections Occasional [Orphanet] 56 / 7739
2
 (HPO:0000795) Abnormality of the urethra Very frequent [Orphanet] 38 / 7739
3
 (HPO:0011830) Abnormality of oral mucosa Very frequent [Orphanet] 47 / 7739
4
 (HPO:0100533) Inflammatory abnormality of the eye Very frequent [Orphanet] 70 / 7739
5
 (HPO:0000613) Photophobia Occasional [Orphanet] 158 / 7739
6
 (HPO:0002754) Osteomyelitis Very frequent [Orphanet] 37 / 7739
7
 (HPO:0100550) Tendon rupture Occasional [Orphanet] 17 / 7739
8
 (HPO:0005059) Arthralgia/arthritis Very frequent [Orphanet] 141 / 7739
9
 (HPO:0100773) Cartilage destruction Very frequent [Orphanet] 7 / 7739
10
 (HPO:0100769) Synovitis Very frequent [Orphanet] 86 / 7739
11
 (HPO:0001387) Joint stiffness Very frequent [Orphanet] 322 / 7739
12
 (HPO:0002024) Malabsorption Very frequent [Orphanet] 142 / 7739
13
 (HPO:0002027) Abdominal pain Frequent [Orphanet] 184 / 7739
14
 (HPO:0002037) Inflammation of the large intestine Frequent [Orphanet] 25 / 7739
15
 (HPO:0004325) Decreased body weight Occasional [Orphanet] 492 / 7739
16
 (HPO:0001805) Thick nail Very frequent [Orphanet] 96 / 7739
17
 (HPO:0000962) Hyperkeratosis Very frequent [Orphanet] 216 / 7739
18
 (HPO:0001597) Abnormality of the nail Very frequent [Orphanet] 115 / 7739
19
 (HPO:0200039) Pustule Very frequent [Orphanet] 20 / 7739
20
 (HPO:0001646) Abnormality of the aortic valve Occasional [Orphanet] 55 / 7739
21
 (HPO:0001697) Abnormality of the pericardium Occasional [Orphanet] 52 / 7739
22
 (HPO:0001945) Fever Occasional [Orphanet] 218 / 7739
23
 (HPO:0011227) Elevated C-reactive protein level Very frequent [Orphanet] 55 / 7739
24
 (HPO:0002103) Abnormality of the pleura Frequent [Orphanet] 58 / 7739
25
 (HPO:0002093) Respiratory insufficiency Occasional [Orphanet] 410 / 7739
26
 (HPO:0002206) Pulmonary fibrosis Occasional [Orphanet] 51 / 7739
27
 (HPO:0100686) Enthesitis Very frequent [Orphanet] 5 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: