ORPHA:1831
De Hauwere syndrome
inactive · moved to ORPHA:782Axenfeld-Rieger syndrome
Synonyms: De Hauwere-Chitty syndrome · Iris dysplasia-hypertelorism-deafness syndrome · Iris dysplasia-hypertelorism-hearing loss syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Axenfeld-Rieger syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | De Hauwere syndrome | De Hauwere-Chitty syndrome · Iris dysplasia-hypertelorism-deafness syndrome · Iris dysplasia-hypertelorism-hearing loss syndrome |
| fr | Syndrome de De Hauwere | Syndrome de De Hauwere-Chitty · Syndrome de dysplasie irienne-hypertélorisme-surdité |
| de | De Hauwere-Syndrom | De Hauwere-Chitty-Syndrom · Irisdysplasie - Hypertelorismus - Schwerhörigkeit |
| es | Síndrome de De Hauwere | Displasia del iris-hipertelorismo-hipoacusia · Displasia del iris-hipertelorismo-sordera · Síndrome de De Hauwere-Chitty |
| it | Sindrome di De Hauwere | Displasia iridea - ipertelorismo - sordità · Sindrome di De Hauwere-Chitty |
| nl | Syndroom van De Hauwere | Irisdysplasie - hypertelorisme - doofheid-syndroom · Irisdysplasie - hypertelorisme - gehoorverlies-syndroom · Syndroom van De Hauwere-Chitty |
| pt | Síndrome De Hauwere | Displasia da íris-hipertelorismo-surdez · Síndrome De Hauwere-Leroy-Adriaenssens |
| pl | Zespół De Hauwere | Dysplazja tęczówki - hipertelozryzm - głuchota · Zespół De Hauwere i Chitty |
| cs | De Hauwerův syndrom | Syndrom zahrnující dysplázii duhovky, hypertelorismus a hluchotu · De Hauwerův-Chittyův syndrom · De Hauwere-Chittyův syndrom |
| uk | Синдром де Хаувера | Синдром де Хаувера-Чітті · Синдром дисплазії райдужки-гіпертелоризму-глухоти · Синдром дисплазії райдужної оболонки - гіпертелоризму - втрати слуху |
| zh | De Hauwere综合征 | 虹膜发育不良-眼距过宽-听力丧失综合征 |
| tr | De Hauwere sendromu | De Hauwere-Chitty sendromu · İris displazisi-hipertelorizm-sağırlık sendromu · İris displazisi-hipertelorizm-işitme kaybı sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 109120 | E | validated | |
| MeSH | C535537 | E | validated | |
| UMLS | C2930925 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Not placed in any Orphanet classification in this release.
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
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/1831
- This record as JSON: /data/d/1831.json