ORPHA:98610
Rare disorder with conjunctival involvement as a major feature
- 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 | Rare disorder with conjunctival involvement as a major feature | |
| fr | Maladie rare avec atteinte conjonctivale comme manifestation majeure | |
| de | Bindehautkrankheit, seltene | |
| es | Enfermedad rara de la conjuntiva | |
| it | Malattia congiuntivale rara | |
| nl | Zeldzame aandoening met betrokkenheid van conjunctiva als hoofdkenmerk | |
| pt | Doença rara com envolvimento da conjuntiva como característica principal | |
| pl | Rzadka choroba spojówki | |
| cs | Vzácná onemocnění spojivky | |
| uk | Рідкісний розлад із залученням конюнктиви як основної ознаки | |
| zh | 罕见结膜受累为主要表现疾病 | |
| tr | Esas klinik özelliği konjonktiva tutulumu olan nadir bozukluk |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681650 | 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:519284Rare disorder of the anterior segment of the eye
rare ophthalmic disorders
Codes that Orphanet moved or referred to this one:
- ORPHA:98611OBSOLETE: Conjunctival vascular anomaly referred to · inactive
- ORPHA:98612OBSOLETE: Conjunctival hemangioma or hemolymphangioma referred to · inactive
- ORPHA:98613OBSOLETE: Conjunctival telangiectasia referred to · inactive
- ORPHA:98614OBSOLETE: Conjunctival lymphangiectasia referred to · inactive
- ORPHA:98615OBSOLETE: Pigmented conjunctival lesion 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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98610
- This record as JSON: /data/d/98610.json