ORPHA:398091
Secondary neonatal autoimmune disease
Synonyms: Transplacentally acquired neonatal autoimmune disease
- Type
- Category
- Group
- Group of disorders
- Age of onset
- Neonatal
- 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 | Secondary neonatal autoimmune disease | Transplacentally acquired neonatal autoimmune disease |
| fr | Maladie auto-immune néonatale secondaire | Maladie auto-immune néonatale par passage transplacentaire d'anticorps |
| de | Sekundäre neonatale autoimmune Krankheit | Transplazentar erworbene neonatale autoimmune Krankheit |
| es | Enfermedad autoinmune neonatal secundaria | Enfermedad autoinmune neonatal adquirida por vía transplacentaria |
| it | Malattia autoimmune neonatale secondaria | Malattia autoimmune neonatale acquisita per via transplacentale |
| nl | Secundaire neonatale auto-immune ziekte | Transplacentair verworven neonatale auto-immune ziekte |
| pt | Doença autoimune neonatal secundária | |
| pl | Wtórna choroba autoimmunologiczna noworodków | Nabyta przezłożyskowa choroba autoimmunologiczna noworodków |
| cs | Sekundární neonatální autoimunitní onemocnění | Transplacentárně získané neonatální autoimunitní onemocnění |
| uk | Вторинне неонатальне аутоімунне захворювання | Трансплацентарно набуте неонатальне аутоімунне захворювання |
| zh | 继发性新生儿自身免疫性疾病 | 经胎盘获得性新生儿自身免疫性疾病 |
| tr | Sekonder yenidoğan otoimmün hastalığı | Transplasental olarak edinsel yenidoğan otoimmün hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0018356 | E | validated | |
| MONDO | 18356 | E | validated | |
| UMLS | C5680041 | 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 (2):
- ORPHA:280373Rare pediatric systemic disease
rare systemic or rheumatologic diseases of childhood - ORPHA:182228Systemic autoimmune disease
rare systemic and rheumatological diseases
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/398091
- This record as JSON: /data/d/398091.json