ORPHA:182228
Systemic autoimmune 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 | Systemic autoimmune disease | |
| fr | Maladie systémique auto-immune | |
| de | Autoimmune Krankheit, systemische | |
| es | Enfermedad autoinmune sistémica | |
| it | Malattia autoimmune sistemica | |
| nl | Systemische auto-immuunziekte | |
| pt | Doença autoimune sistémica | |
| pl | Układowa choroba autoimmunologiczna | |
| cs | Systémová autoimunitní onemocnění | |
| uk | Системне аутоімунне захворювання | |
| zh | 系统性自身免疫性疾病 | |
| tr | Sistemik otoimmün hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15939 | E | validated | |
| UMLS | C2895206 | 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:182222Rare systemic disease
rare systemic and rheumatological diseases
Children (24):
- ORPHA:80Antiphospholipid syndrome
- ORPHA:444463Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiency
- ORPHA:444092Autoimmune interstitial lung disease-arthritis syndrome
- ORPHA:300345Autosomal systemic lupus erythematosus
- ORPHA:464343Catastrophic antiphospholipid syndrome
- ORPHA:481662Familial Chilblain lupus
- ORPHA:98482Idiopathic inflammatory myopathy
- ORPHA:284264IgG4-related disease
- ORPHA:251312Overlapping connective tissue disease
- ORPHA:300359PLCG2-associated antibody deficiency and immune dysregulation
- ORPHA:93552Pediatric systemic lupus erythematosus
- ORPHA:289390Primary Sjögren disease
- ORPHA:728Relapsing polychondritis
- ORPHA:247691Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
- ORPHA:779Reynolds syndrome
- ORPHA:438159STAT3-related early-onset multisystem autoimmune disease
- ORPHA:3130Satoyoshi syndrome
- ORPHA:398091Secondary neonatal autoimmune disease
- ORPHA:820Sneddon syndrome
- ORPHA:838Susac syndrome
- ORPHA:228426Syndromic multisystem autoimmune disease due to Itch deficiency
- ORPHA:536Systemic lupus erythematosus
- ORPHA:90291Systemic sclerosis
- ORPHA:90002Undifferentiated connective tissue 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/182228
- This record as JSON: /data/d/182228.json