ORPHA:1135
Arrhinia-choanal atresia-microphthalmia syndrome
inactive · moved to ORPHA:2250Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism 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 Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Arrhinia-choanal atresia-microphthalmia syndrome | |
| fr | Syndrome d'arhinie-atrésie des choanes-microphtalmie | |
| de | Arrhinie-Choanalatresie-Mikrophthalmie-Syndrom | |
| es | Síndrome de arrinia-atresia de coanas-microftalmia | |
| it | Arinia - atresia delle coane - microftalmia | |
| nl | Arrhinie - choane atresie - microftalmie-syndroom | |
| pt | Síndrome de arrinia-atresia das coanas-microftalmia | |
| pl | Brak nosa - atrezja nozdrzy tylnych - mikroftalmia | |
| cs | Syndrom zahrnující arhinii, atrézii choan a mikroftalmii | |
| uk | Синдром аррінії-хоанальної атрезії-мікрофтальмії | |
| zh | 无鼻畸形-鼻后孔闭锁-小眼畸形综合征 | |
| tr | Arini-koanal atrezi-mikroftalmi sendromu |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0015238 | E | validated | |
| UMLS | C1863878 | E | validated | |
| GARD | 8755 | 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.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/1135
- This record as JSON: /data/d/1135.json