ORPHA:486955
Rare pediatric 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare pediatric rheumatologic disease | |
| fr | Maladie rhumatologique rare de l'enfant | |
| de | Seltene pädiatrische rheumatologische Krankheit | |
| es | Enfermedad reumatológica pediátrica rara | |
| it | Malattia reumatica pediatrica rara | |
| nl | Zeldzame pediatrische reumatologische ziekte | |
| pt | Doença reumatológica pediátrica rara | |
| pl | Rzadkie dziecięce choroby reumatologiczne | |
| cs | Vzácná pediatrická revmatologická onemocnění | |
| uk | Рідкісне дитяче ревматологічне захворювання | |
| zh | 罕见的儿童风湿病 | |
| tr | Nadir pediatrik romatolojik hastalık |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681264 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:280342Rare systemic or rheumatological disease of childhood
rare systemic or rheumatologic diseases of childhood
Children (9):
- ORPHA:319719Autoinflammatory syndrome of childhood
- ORPHA:477650Fibroblastic rheumatism
- ORPHA:73Gorham-Stout disease
- ORPHA:955Hajdu-Cheney syndrome
- ORPHA:85193Idiopathic juvenile osteoporosis
- ORPHA:329967Intermittent hydrarthrosis
- ORPHA:92Juvenile idiopathic arthritis
- ORPHA:29207Reactive arthritis
- ORPHA:793SAPHO 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/486955
- This record as JSON: /data/d/486955.json