OBSOLETE: Autosomal recessive hyper-IgE syndrome
inactive · referred to ORPHA:641368Autosomal recessive hyper-IgE syndrome due to ZNF341 deficiency
Synonyms: OBSOLETE: AR-HIES · OBSOLETE: Autosomal recessive HIES · OBSOLETE: Hyperimmunoglobulin E syndrome type 2 · OBSOLETE: Non-skeletal hyper-IgE syndrome
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Autosomal recessive hyper-IgE syndrome due to ZNF341 deficiency
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Autosomal recessive hyper-IgE syndrome | OBSOLETE: AR-HIES · OBSOLETE: Autosomal recessive HIES · OBSOLETE: Hyperimmunoglobulin E syndrome type 2 · OBSOLETE: Non-skeletal hyper-IgE syndrome |
| fr | OBSOLETE : Syndrome hyper-IgE autosomique récessif | OBSOLETE : HIES autosomique recessif · OBSOLETE : Syndrome d'hyper IgE non squelettique · OBSOLETE : Syndrome d'hyperimmunoglobuline E type 2 |
| de | OBSOLET: Hyper IgE-Syndrom, autosomal-rezessives | OBSOLET: AR-HIES · OBSOLET: HIES, autosomal-rezessives · OBSOLET: Hyper IgE-Syndrom, nicht-skelettales · OBSOLET: Hyperimmunoglobulinämie E-Syndrom Typ 2 |
| es | OBSOLETO: Síndrome de hiper-IgE autosómico recesivo | OBSOLETO: HIES autosómica recesiva · OBSOLETO: Síndrome de hiperinmunoglobulina E tipo 2 · OBSOLETO: Síndrome hiper IgE no esquelético |
| it | OBSOLETO: Sindrome da iper-IgE autosomica recessiva | OBSOLETO: AR-HIES · OBSOLETO: HIES autosomica recessiva · OBSOLETO: Sindrome da iper-IgE non scheletrica · OBSOLETO: Sindrome da iperimmunoglobulinemia E, tipo 2 |
| nl | OBSOLEET: Autosomaal recessief hyper-IgE-syndroom | OBSOLEET: AR-HIES · OBSOLEET: Autosomaal recessief HIES · OBSOLEET: Hyperimmunoglobuline-E-syndroom type 2 · OBSOLEET: Niet-skeletaal hyper-IgE-syndroom |
| pt | OBSOLETO: Síndrome hiper-IgE autossómica recessiva | |
| pl | NIEAKTUALNE: Autosomalny recesywny zespól hiper IgE | NIEAKTUALNE: AR-HIES · NIEAKTUALNE: Autosomalny recesywny HIES · NIEAKTUALNE: Nieszkieletowy zespół hiper IgE · NIEAKTUALNE: Zespół hiperimmunoglobuliny E typu 2 |
| cs | NEAKTUÁLNÍ: Autozomálně recesivní syndrom hyper-IgE | = en |
| uk | ЗАСТАРІЛО: Аутосомно-рецесивний синдром гіпер-IgE | ЗАСТАРІЛО: AR-HIES · ЗАСТАРІЛО: Аутосомно-рецесивний HIES · ЗАСТАРІЛО: Синдром гіперімуноглобуліну Е, тип 2 · ЗАСТАРІЛО: Нескелетний синдром гіпер-IgE |
| zh | 弃用：常染色体隐性高免疫球蛋白E综合征 | 高免疫球蛋白E综合征2型 |
| tr | Eski adı: Otozomal resesif hiper-IgE sendromu | AR-HIES · Otozomal çekinik HIES · İskelet dışı hiper-IgE sendromu · Hiperimmünoglobulin E sendromu tip 2 |
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
Classification
Not placed in any Orphanet classification in this release.
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/169446
- This record as JSON: /data/d/169446.json