ORPHA:101950
Rare eye tumor
- 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 eye tumor | |
| fr | Tumeur rare de l'oeil | Tumeur rare des yeux |
| de | Augentumor, seltener | |
| es | Tumor ocular raro | |
| it | Tumore oculare | |
| nl | Zeldzame oogtumor | |
| pt | Tumor ocular | |
| pl | Rzadkie guzy oczu | |
| cs | Vzácný nádor oka | |
| uk | Рідкісна пухлина ока | |
| zh | 罕见眼肿瘤 | |
| tr | Nadir göz tümörü |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15121 | E | validated | |
| UMLS | C5681794 | E | validated | |
| GARD | 19795 | 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 (2):
- ORPHA:97966Rare ophthalmic disorder
rare ophthalmic disorders - ORPHA:98057Rare tumor
rare neoplastic diseases
Children (15):
- ORPHA:440727Combined hamartoma of the retina and retinal pigment epithelium
- ORPHA:617910Conjunctival malignant melanoma
- ORPHA:658590Eyelid sebaceous carcinoma
- ORPHA:268139Intraocular medulloepithelioma
- ORPHA:723195Iris melanoma
- ORPHA:715862Melanocytoma of the optic disc and optic nerve
- ORPHA:636Neurofibromatosis type 1
- ORPHA:659744Ocular surface squamous neoplasia
- ORPHA:52994Orbital leiomyoma
- ORPHA:279897Primary oculocerebral lymphoma
- ORPHA:716204Rare neoplastic choroidal disorder
- ORPHA:716198Rare paraneoplastic choroidal disorder
- ORPHA:790Retinoblastoma
- ORPHA:91481Ring dermoid of cornea
- ORPHA:353356Vasoproliferative tumor of the retina
Codes that Orphanet moved or referred to this one:
- ORPHA:39044OBSOLETE: Uveal melanoma referred to · inactive
- ORPHA:98580OBSOLETE: Palpebral tumor referred to · inactive
- ORPHA:98581OBSOLETE: Palpebral epidermal tumor referred to · inactive
- ORPHA:98582OBSOLETE: Benign tumor of palpebral epidermis referred to · inactive
- ORPHA:98583OBSOLETE: Precancerous lesion of palpebral epidermis referred to · inactive
- ORPHA:98584OBSOLETE: Malignant tumor of palpebral epidermis referred to · inactive
- ORPHA:98585OBSOLETE: Palpebral sebaceous gland tumor referred to · inactive
- ORPHA:98586OBSOLETE: Pigmented palpebral tumor referred to · inactive
- ORPHA:98587OBSOLETE: Palpebral lentiginosis referred to · inactive
- ORPHA:98589OBSOLETE: Palpebral malignant melanoma referred to · inactive
- ORPHA:98590OBSOLETE: Palpebral piliary tumor referred to · inactive
- ORPHA:98591OBSOLETE: Mesenchymatous palpebral tumor referred to · inactive
- ORPHA:98592OBSOLETE: Palpebral tumor with a vascular malformation referred to · inactive
- ORPHA:98593OBSOLETE: Neurogenic palpebral tumor referred to · inactive
- ORPHA:98616OBSOLETE: Conjunctival tumor referred to · inactive
- ORPHA:98617OBSOLETE: Bulbar conjunctival dermoid or conjunctival dermolipoma referred to · inactive
- ORPHA:98703OBSOLETE: Disease with potential neoplastic degeneration associated with ocular features 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/101950
- This record as JSON: /data/d/101950.json