ORPHA:98635
Corneodysgenesis
Synonyms: Corneogoniodysgenesis
- 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 | Corneodysgenesis | Corneogoniodysgenesis |
| fr | Cornéo-dysgénésie | Cornéo-gonio-dysgénésie |
| de | Corneogoniodysgenesie | |
| es | Corneogoniodisgenesia | |
| it | Corneogoniodisgenesia | |
| nl | Corneogoniodysgenesie | |
| pt | Corneogoniodisgenesia | |
| pl | Korneogoniodysgeneza | = en |
| cs | Dysgeneze rohovky a komorového úhlu | = en |
| uk | Корнеодисгенез | Корнеогоніодисгенез |
| zh | 角膜发育不全 | 角膜前房角发育不全 |
| tr | Korneodisgenezi | Korneogoniodisgenezi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680334 | 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 (4):
- ORPHA:98553Developmental defect of the eye
rare developmental anomalies during embryogenesis - ORPHA:183557Genetic developmental defect of the eye
rare genetic diseases - ORPHA:519282Rare corneal disorder
rare ophthalmic disorders - ORPHA:522556Rare genetic corneal disorder
rare genetic diseases
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/98635
- This record as JSON: /data/d/98635.json