ORPHA:3022
Rapp-Hodgkin syndrome
inactive · moved to ORPHA:1071Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
Synonyms: Ectodermal dysplasia syndrome, Rapp-Hodgkin type · Ectodermal dysplasia, Rapp-Hodgkin type · Hypohidrotic ectodermal dysplasia- cleft lip/palate syndrome · RHS
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rapp-Hodgkin syndrome | Ectodermal dysplasia syndrome, Rapp-Hodgkin type · Ectodermal dysplasia, Rapp-Hodgkin type · Hypohidrotic ectodermal dysplasia- cleft lip/palate syndrome · RHS |
| fr | Syndrome de Rapp-Hodgkin | Dysplasie ectodermique type Rapp-Hodgkin · Syndrome de dysplasie ectodermique hypohidrotique-fente labiale/palatine |
| de | Rapp-Hodgkin-Syndrom | Ektodermale Dysplasie Typ Rapp-Hodgkin · Hypohidrotische ektodermale Dysplasie-Lippengaumenspalte-Syndrom · RHS |
| es | Síndrome de Rapp-Hodgkin | Displasia ectodérmica tipo Rapp-Hodgkin · Síndrome de displasia ectodérmica hipohidrótica-fisura labiopalatina · Síndrome de displasia ectodérmica tipo Rapp-Hodgkin |
| it | Sindrome di Rapp-Hodgkin | Displasia ectodermica, tipo Rapp-Hodgkin · RHS · Sindrome da displasia ectodermica, tipo Rapp-Hodgkin · Sindrome displasia ectodermica anidrotica-labio/palatoschisi |
| nl | Syndroom van Rapp-Hodgkin | Ectodermale dysplasie, Rapp-Hodgkin-type · Ectodermale dysplasie-syndroom, Rapp-Hodgkin-type · Hypohidrotische ectodermale dysplasie - gespleten lip/gehemelte-syndroom · RHS |
| pt | Síndrome Rapp-Hodgkin | Displasia ectodérmica, tipo Rapp-Hodgkin · RHS · Síndrome de displasia ectodérmica hipohidrótica-fenda labiopalatina · Síndrome de displasia ectodérmica, tipo Rapp-Hodgkin |
| pl | Zespół Rappa i Hodgkina | Dysplazja ektodermalna, typ Rappa i Hodgkina · RHS · Zespół anhydrotycznej dysplazji ektodermalnej i rozszczepu wargi/podniebienia · Zespół dysplazji ektodermalnej, typ Rappa i Hodgkina |
| cs | Rappův-Hodgkinův syndrom | RHS · Syndrom zahrnující anhidrotickou ektodermální dysplázii a rozštěp rtu/patra · Syndrom ektodermální dysplázie, Rappův-Hodgkinův typ · Ektodermální dysplázie, Rappův-Hodgkinův typ · Rapp-Hodgkinův syndrom · Syndrom ektodermální dysplázie, Rapp-Hodgkinův typ · Ektodermální dysplázie, Rapp-Hodgkinův typ |
| uk | Синдром Раппа-Ходжкіна | Синдром ангідротичної ектодермальної дисплазії - розщілини губи/піднебіння · Синдром ектодермальної дисплазії, тип Раппа-Ходжкіна · Ектодермальна дисплазія, тип Раппа-Ходжкіна · RHS |
| zh | 桡骨侧列缺损-髌骨发育不全-腭裂或高度拱形腭裂-腹泻-关节脱位-矮小四肢畸形-鼻子细长但智力正常 | 无汗性外胚层发育不良-唇腭裂综合征 |
| tr | Rapp-Hodgkin sendromu | RHS · Ektodermal displazi, Rapp-Hodgkin tipi · Ektodermal displazi sendromu, Rapp-Hodgkin tipi · Anhidrotik ektodermik displazi-yarık dudak / damak sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 129400 | E | validated | |
| MeSH | C535289 | E | validated | |
| UMLS | C1785148 | 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
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/3022
- This record as JSON: /data/d/3022.json