ORPHA:98631
Congenital malformation of the eye with glaucoma as a major feature
- Type
- Category
- Group
- Group of disorders
- Status
- active
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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Congenital malformation of the eye with glaucoma as a major feature | |
| fr | Malformation congénitale de l'oeil avec glaucome comme manifestation majeure | |
| de | Glaucoma, secondary dysgenetic | |
| es | Glaucoma disgenético secundario | |
| it | Glaucoma secondario disgenetico | |
| nl | Congenitale malformatie van oog met glaucoom als hoofdkenmerk | |
| pt | Malformação do olho com glaucoma como característica principal | |
| pl | Wtórna jaskra dysgenetyczna | |
| cs | Sekundární glaukom u dysgeneze předního segmentu | |
| uk | Вроджена вада розвитку ока з глаукомою як основною ознакою | |
| zh | 以青光眼为特征先天性眼畸形 | |
| tr | Esas klinik özelliği glokomlu göz olan doğumsal malformasyon |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681671 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:98553Developmental defect of the eye
rare developmental anomalies during embryogenesis - ORPHA:519331Secondary early-onset glaucoma
rare ophthalmic disorders
Children (8):
- ORPHA:98634Anterior segment developmental anomaly without extraocular manifestations
- ORPHA:190Coats disease
- ORPHA:238763Glaucoma secondary to spherophakia/ectopia lentis and megalocornea
- ORPHA:64734Iridocorneal endothelial syndrome
- ORPHA:35612Isolated complete colobomatous microphthalmia
- ORPHA:94058Neovascular glaucoma
- ORPHA:98973Posterior polymorphous corneal dystrophy
- ORPHA:792X-linked retinoschisis
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98631
- This record as JSON: /data/d/98631.json