ORPHA:522532
Rare genetic disorder of the lacrimal apparatus
- 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 lacrimal apparatus | |
| fr | Maladie génétique rare de l'appareil lacrymal | |
| de | Seltene genetische Krankheit des Tränenapparats | |
| es | Trastorno genético raro del aparato lagrimal | |
| it | Malattia genetica rara dell'apparato lacrimale | |
| nl | Zeldzame genetische aandoening van traanapparaat | |
| pt | Doença genética rara do aparelho lacrimal | |
| pl | Rzadka choroba układu łzowego uwarunkowana genetycznie | |
| cs | Vzácná genetická porucha exkrečního aparátu lakrimálního systému | |
| uk | Рідкісне генетично обумовлене захворювання сльозового апарату | |
| zh | 罕见泪腺器官的遗传性疾病 | |
| tr | Lakrimal aparatın nadir genetik bozukluğu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681425 | 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:522524Rare genetic disorder of the ocular adnexa
rare genetic diseases
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/522532
- This record as JSON: /data/d/522532.json