ORPHA:98563
Microblepharon-ablephara syndrome
- Type
- Clinical group
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Microblepharon-ablephara syndrome | |
| fr | Microblépharon-ablépharie | |
| de | Mikroblepharon - Ablepharie | |
| es | Síndrome de microblefaron-ablefaria | |
| it | Microblefaron - ablefaria | |
| nl | Microblefaron - ablephara-syndroom | |
| pt | Microblefaron - ablefaria | |
| pl | Microblepharon - wrodzony małe powieki | |
| cs | Syndromy s hypoplázií/aplázií očních víček | |
| uk | Синдром мікроблефарон-аблефарон | |
| zh | 小眼睑-无睑畸形综合征 | |
| tr | Mikroblefaron-ablefara sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681656 | 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98563
- This record as JSON: /data/d/98563.json