ORPHA:715862
Melanocytoma of the optic disc and optic nerve
Synonyms: Hyperpigmented magnocellular naevus · Magnocellular naevus
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Melanocytoma of the optic disc and optic nerve | Hyperpigmented magnocellular naevus · Magnocellular naevus |
| fr | Mélanocytome du disque optique et du nerf optique | |
| de | Melanozytom des Sehnervenkopfes und des Sehnervs | Hyperpigmentierter magnozellulärer Nävus · Magnozellulärer Naevus |
| es | Melanocitoma del disco y del nervio óptico | Nevo magnocelular · Nevo magnocelular hiperpigmentado |
| it | Melanocitoma del disco ottico e del nervo ottico | Nevo magnocellulare iperpigmentato · Nevo magnocellulare |
| nl | Melanocytoom van papil en nervus opticus | Melanocytoom van blinde vlek en oogzenuw · Hypergepigmenteerde magnocellulaire naevus · Magnocellulaire naevus |
| pt | Melanocytoma of the optic disc and optic nerve | |
| pl | Melanocytoma tarczy nerwu wzrokowego i nerwu wzrokowego | = en |
| cs | Melanocytoma of the optic disc and optic nerve | = en |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:101950Rare eye tumor
rare ophthalmic disorders; rare neoplastic diseases - ORPHA:716296Rare isolated non-progressive predominantly chorioretinal disorder
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
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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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/715862
- This record as JSON: /data/d/715862.json