ORPHA:476102
OBSOLETE: Hereditary pediatric Behçet-like disease
inactive · referred to ORPHA:324936Unclassified autoinflammatory syndrome
Synonyms: OBSOLETE: Behçet-like disease due to HA20 · OBSOLETE: Behçet-like disease due to haploinsufficiency of A20
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Unclassified autoinflammatory syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Hereditary pediatric Behçet-like disease | OBSOLETE: Behçet-like disease due to HA20 · OBSOLETE: Behçet-like disease due to haploinsufficiency of A20 |
| fr | OBSOLETE : Maladie de Behçet-like héréditaire de l'enfant | OBSOLETE : Maladie de Behçet-like par haploinsuffisance de A20 |
| de | OBSOLET: Behçet-ähnliche Krankheit des Kindes, hereditäre | OBSOLET: Behçet-ähnliche Krankheit durch A20-Haploinsuffizienz · OBSOLET: Behçet-ähnliche Krankheit durch HA20 |
| es | OBSOLETO: Enfermedad pediátrica hereditaria similar a Behçet | OBSOLETO: Enfermedad similar a Behçet por HA20 · OBSOLETO: Enfermedad similar a Behçet por haploinsuficiencia de A20 |
| it | OBSOLETO: Malattia pediatrica ereditaria simil-Behçet | OBSOLETO: Malattia simil-Behçet da HA20 · OBSOLETO: Malattia simil-Behçet da aploinsufficienza di A20 · OBSOLETO: Malattia simil-Behçet da HA20 · OBSOLETO: Malattia simil-Behçet da aploinsufficienza di A20 |
| nl | OBSOLEET: Hereditaire pediatrische Behçet-achtige ziekte | OBSOLEET: Behçet-achtige ziekte door A20-haploinsufficiëntie · OBSOLEET: Behçet-achtige ziekte door HA20 |
| pt | OBSOLETO: Doença pediátrica hereditária Behçet-like | OBSOLETO: Doença Behçet-like devido a HA20 · OBSOLETO: Doença Behçet-like devido a haploinsuficiência A20 |
| pl | NIEAKTUALNE: Dziedziczna choroba Behþeta u dzieci i młodzieży | NIEAKTUALNE: Choroba podobna do choroby Behçeta spowodowana HA20 · NIEAKTUALNE: Choroba podobna do choroby Behçeta spowodowana haploinsuficjencją A20 |
| cs | NEAKTUÁLNÍ: Dědičné dětské onemocnění podobné Behçetově nemoci | NEAKTUÁLNÍ: Behçet-like disease due to HA20 · NEAKTUÁLNÍ: Behçet-like disease due to haploinsufficiency of A20 · NEAKTUÁLNÍ: Behçet-like onemocnění způsobené HA20 · NEAKTUÁLNÍ: Behçet-like onemocnění způsobené haploinsuficiencí A20 |
| uk | ЗАСТАРІЛО: Спадкова дитяча Бехчет-подібна хвороба | ЗАСТАРІЛО: Бехчет-подібна хвороба, спричинена HA20 · ЗАСТАРІЛО: Бехчет-подібна хвороба, спричинена гаплонедостатністю А20 |
| zh | 遗传性儿科Behpet样疾病 | A20单倍剂量不足导致的Behcet样疾病 |
| tr | Kalıtsal pediatrik Behçet-benzeri hastalık | HA20'ye bağlı Behçet benzeri hastalık · A20'nin haplo yetersizliğine bağlı Behçet benzeri hastalık |
Definition in:
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/476102
- This record as JSON: /data/d/476102.json