ORPHA:98565
Syndromic ankyloblepharon filiforme adnatum
Synonyms: Syndromic ankyloblepharon
- 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 | Syndromic ankyloblepharon filiforme adnatum | Syndromic ankyloblepharon |
| fr | Ankyloblépharon filiforme adnatum syndromique | Ankyloblépharon syndromique |
| de | Ankyloblepharon, syndromales | |
| es | Anquilobléfaron sindrómico | |
| it | Anchiloblefaron sindromico | |
| nl | Syndromaal ankyloblefaron | |
| pt | Anquiloblefaron filiforme adnatum sindromático | Anquiloblefaron sindromático |
| pl | Syndromiczne zrośnięcie brzegów powiek | = en |
| cs | Syndromy se srůsty víček | = en |
| uk | Синдромальний філігранний анкілоблефарон (ankyloblepharon filiforme adnatum) | Синдромальний анкілоблефарон |
| zh | 综合征性丝状睑缘粘连 | 综合征性睑缘粘连 |
| tr | Sendromik ankiloblefaron filiforme adnatum | Sendromik ankiloblefaron |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680329 | 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:98564Eyelid border anomaly
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/98565
- This record as JSON: /data/d/98565.json