01
- Entity Type
- Diseases
- Relation Groups
- 3
- Relation Preview
- 24
Basic Information
Grouped by core information, identifiers, and descriptions.
Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.
Core Information
- Disease Name
- Reiter Syndrome
- Standard Disease Name
- reiter syndrome
- MeSH Tree
- No data
- ICD-10
- M02.3|M02.30
Identifiers
- DO ID
- No data
- MeSH ID
- D016918
- OMIM ID
- No data
- UMLS ID
- C0035012
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_02D:A rare, reactive inflammatory disorder seen following bacterial infection. It predominantly affects males aged 20-40. Individuals with HLA-B27 antigen are estimated to have a 50 % increased risk. The disorder is characterized by arthritis, conjunctivitis, uveitis, iritis and ulceration of the oral cavity, genitals and volar surfaces of the hands and feet. The clinical course is self-limited with resolution of clinical disease usually within six months of onset.|MSH2017_2016_08_12:Historically characterized by a triad of inflammation involving the eye (CONJUNCTIVITIS), the bone (POST-INFECTIOUS ARTHRITIS), and the urethra (URETHRITIS), it is now thought to be nearly synonymous with reactive arthritis.|CSP2006:triad of nongonococcal urethritis followed by conjunctivitis and arthritis.