ORPHA:182222
Rare 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 systemic disease | |
| fr | Maladie systémique rare | |
| de | Seltene systemische Krankheit | |
| es | Enfermedad rara sistémica | |
| it | Malattia sistemica rara | |
| nl | Zeldzame systemische ziekte | |
| pt | Doença sistémica rara | |
| pl | Rzadka choroba układowa | |
| cs | Vzácná systémová onemocnění | |
| uk | Рідкісне системне захворювання | |
| zh | 罕见系统性疾病 | |
| tr | Nadir sistemik hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680585 | 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 (35):
- ORPHA:69Amyloidosis
- ORPHA:280062Calciphylaxis
- ORPHA:300284Connective tissue disorder due to lysyl hydroxylase-3 deficiency
- ORPHA:231111Drug-induced lupus erythematosus
- ORPHA:98249Ehlers-Danlos syndrome
- ORPHA:230857Ehlers-Danlos/osteogenesis imperfecta syndrome
- ORPHA:2295Familial articular hypermobility syndrome
- ORPHA:337Fibrodysplasia ossificans progressiva
- ORPHA:697101Fontaine progeroid syndrome
- ORPHA:774Hereditary hemorrhagic telangiectasia
- ORPHA:722Hypoplasminogenemia
- ORPHA:50918Kikuchi-Fujimoto disease
- ORPHA:482Kimura disease
- ORPHA:521450LAMA5-related multisystemic syndrome
- ORPHA:389Langerhans cell histiocytosis
- ORPHA:158061Macrophage activation syndrome
- ORPHA:679Malignant atrophic papulosis
- ORPHA:284993Marfan syndrome and Marfan-related disorders
- ORPHA:598363Multisystem inflammatory syndrome in children and adults
- ORPHA:2582Myalgia-eosinophilia syndrome associated with tryptophan
- ORPHA:157987Non-Langerhans cell histiocytosis
- ORPHA:279947Postorgasmic illness syndrome
- ORPHA:300382Progeroid and marfanoid aspect-lipodystrophy syndrome
- ORPHA:764Pyomyositis
- ORPHA:3018Retinal ischemic syndrome-digestive tract small vessel hyalinosis-diffuse cerebral calcifications syndrome
- ORPHA:3096Reye syndrome
- ORPHA:3099Rheumatic fever
- ORPHA:797Sarcoidosis
- ORPHA:90051Sepsis in premature infants
- ORPHA:182228Systemic autoimmune disease
- ORPHA:188Systemic capillary leak syndrome
- ORPHA:542323T-cell based immunotherapy-associated cytokine release syndrome
- ORPHA:457077TAFRO syndrome
- ORPHA:284227TEMPI syndrome
- 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/182222
- This record as JSON: /data/d/182222.json