ORPHA:280373
Rare pediatric systemic 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 pediatric systemic disease | |
| fr | Maladie systémique rare de l'enfant | |
| de | Seltene systemische Krankheit des Kindes | |
| es | Enfermedad sistémica pediátrica rara | |
| it | Malattia sistemica pediatrica | |
| nl | Zeldzame pediatrische systemische ziekte | |
| pt | Doença sistémica pediátrica rara | |
| pl | Rzadka dziecięca choroba układowa | |
| cs | Systémová onemocnění v pediatrii | |
| uk | Рідкісне дитяче системне захворювання | |
| zh | 罕见小儿系统性疾病 | |
| tr | Nadir pediatrik sistemik hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680784 | 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:280342Rare systemic or rheumatological disease of childhood
rare systemic or rheumatologic diseases of childhood
Children (15):
- ORPHA:444463Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiency
- ORPHA:444092Autoimmune interstitial lung disease-arthritis syndrome
- ORPHA:3165Eosinophilic fasciitis
- ORPHA:337Fibrodysplasia ossificans progressiva
- ORPHA:93672Juvenile dermatomyositis
- ORPHA:93568Juvenile polymyositis
- ORPHA:598363Multisystem inflammatory syndrome in children and adults
- ORPHA:251312Overlapping connective tissue disease
- ORPHA:300359PLCG2-associated antibody deficiency and immune dysregulation
- ORPHA:93552Pediatric systemic lupus erythematosus
- ORPHA:438159STAT3-related early-onset multisystem autoimmune disease
- ORPHA:797Sarcoidosis
- ORPHA:398091Secondary neonatal autoimmune disease
- ORPHA:90291Systemic sclerosis
- ORPHA:251332Unexplained long-lasting fever/inflammatory 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/280373
- This record as JSON: /data/d/280373.json