ORPHA:99177
Isolated distichiasis
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
Isolated distichiasis is a rare congenital eyelid anomaly characterized by an accessory row of eyelashes (that may be partial or complete) posterior to the normal row of cilia, at or close to the meibomian gland orifices, that is not associated with any other condition, and that may lead to ocular irritation and corneal damage if left untreated.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Isolated distichiasis | |
| fr | Distichiasis isolé | |
| de | Distichiasis, isolierte | |
| es | Distiquiasis aislada | |
| it | Distichiasi isolata | |
| nl | Geïsoleerde distichiase | |
| pt | Distiquíase | |
| pl | Izolowana dwurzędowość rzęs | |
| cs | Izolovaná distichiáza | |
| uk | Ізольований дистихіоз | |
| zh | 孤立型双睫症 | |
| tr | İzole distikiyaz |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 126300 | E | validated | |
| ICD-10 | Q10.3 | NTBT | attributed | validated |
| ICD-11 | LA14.0Y | NTBT | index | validated |
| MONDO | 0007464 | E | validated | |
| UMLS | C5779555 | E | validated | |
| MedDRA | 10066128 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98594Rare eyebrow/eyelash disorder
rare developmental anomalies during embryogenesis; rare genetic diseases; rare ophthalmic disorders
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/99177
- This record as JSON: /data/d/99177.json