ORPHA:522524
Rare genetic disorder of the ocular adnexa
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare genetic disorder of the ocular adnexa | |
| fr | Maladie génétique rare de l'annexe oculaire | |
| de | Seltene genetische Krankheit der okularen Adnexe | |
| es | Trastorno genético raro de los anexos oculares | |
| it | Malattia genetica rara degli annessi oculari | |
| nl | Zeldzame genetische aandoening van adnex van oog | |
| pt | Doença genética rara dos anexos oculares | |
| pl | Rzadka choroba przydatków oka uwarunkowna genetycznie | |
| cs | Vzácná genetická porucha očních adnex | |
| uk | Рідкісне генетично обумовлене захворювання очного яблука | |
| zh | 罕见眼附属器遗传性疾病 | |
| tr | Oküler adneksin nadir genetik bozukluk |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681430 | 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:522504Rare genetic disorder of the visual organs
rare genetic diseases
Codes that Orphanet moved or referred to this one:
- ORPHA:183598OBSOLETE: Rare genetic palpebral, lacrimal system and conjunctival disease referred to · inactive
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/522524
- This record as JSON: /data/d/522524.json