ORPHA:140653
Neuro-ophthalmological disease
- 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 | Neuro-ophthalmological disease | |
| fr | Maladie neuro-ophtalmologique | |
| de | Neuro-ophthalmologische Krankheit | |
| es | Enfermedad neuro-oftalmológica | |
| it | Malattia neuro-oftalmica | |
| nl | Neuro-oftalmologische ziekte | |
| pt | Doença neuro-oftalmológica | |
| pl | Choroba neurooftalmologiczna | |
| cs | Neuro-oftalmologická onemocnění | |
| uk | Нейроофтальмологічні захворювання | |
| zh | 神经-眼病 | |
| tr | Nöro-oftalmolojik hastalık |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15368 | E | validated | |
| UMLS | C5680678 | E | validated | |
| GARD | 19930 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:520814Rare disorder of the visual organs
rare ophthalmic disorders
Codes that Orphanet moved or referred to this one:
- ORPHA:98691OBSOLETE: Abnormal eye movements referred to · inactive
- ORPHA:98692OBSOLETE: Nervous system anomaly with eye involvement referred to · inactive
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/140653
- This record as JSON: /data/d/140653.json