ORPHA:182231
Rare rheumatologic disease
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare rheumatologic disease | |
| fr | Maladie rhumatologique rare | |
| de | Seltene rheumatologische Krankheit | |
| es | Enfermedad reumatológica rara | |
| it | Malattia reumatologica rara | |
| nl | Zeldzame reumatologische ziekte | |
| pt | Doença reumatológica rara | |
| pl | Rzadka choroba reumatologiczna | |
| cs | Vzácná revmatologická onemocnění | |
| uk | Рідкісне ревматологічне захворювання | |
| zh | 罕见风湿病 | |
| tr | Nadir romatolojik hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15940 | E | validated | |
| UMLS | C5680586 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98023Rare systemic or rheumatologic disease
rare systemic and rheumatological diseases
Children (21):
- ORPHA:829Adult-onset Still disease
- ORPHA:93665Autoinflammatory syndrome
- ORPHA:2848Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome
- ORPHA:658951Early-onset immune dysregulation due to DOCK11 complete deficiency
- ORPHA:1416Familial calcium pyrophosphate deposition
- ORPHA:47612Felty syndrome
- ORPHA:477650Fibroblastic rheumatism
- ORPHA:73Gorham-Stout disease
- ORPHA:662255Grisel syndrome
- ORPHA:955Hajdu-Cheney syndrome
- ORPHA:85193Idiopathic juvenile osteoporosis
- ORPHA:714829Immune checkpoint inhibitor-induced myositis
- ORPHA:238569Immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections syndrome
- ORPHA:529977Immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections-lymphopenia syndrome
- ORPHA:329967Intermittent hydrarthrosis
- ORPHA:79099Interstitial granulomatous dermatitis with arthritis
- ORPHA:178311Isolated sternocostoclavicular hyperostosis
- ORPHA:92Juvenile idiopathic arthritis
- ORPHA:399158Osteonecrosis
- ORPHA:29207Reactive arthritis
- ORPHA:658584Rowell syndrome
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/182231
- This record as JSON: /data/d/182231.json