ORPHA:98562
Cryptophthalmia
- 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 | Cryptophthalmia | |
| fr | Cryptophtalmie | |
| de | Kryptophthalmie | |
| es | Criptoftalmia | |
| it | Criptoftalmia | |
| nl | Cryptoftalmie | |
| pt | Criptoftalmia | |
| pl | Skrytoocze | |
| cs | Kryptoftalmie | |
| uk | Криптофтальмія | |
| zh | 隐眼 | |
| tr | Kriptoftalmi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | LA14.01 | E | specific | validated |
| MONDO | 0020153 | E | validated | |
| UMLS | C0311249 | E | validated | |
| GARD | 10505 | E | validated | |
| MedDRA | 10011497 | 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 (1):
- ORPHA:98561Congenital malformation of the eyelid
rare developmental anomalies during embryogenesis; rare genetic diseases; rare ophthalmic disorders
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/98562
- This record as JSON: /data/d/98562.json