ORPHA:519349
Rare ophthalmic disorder with cranial nerve involvement
- 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 ophthalmic disorder with cranial nerve involvement | |
| fr | Maladie rare ophtalmique avec atteinte des nerfs crâniens | |
| de | Seltene Augenkrankheit mit Hirnnervenbeteiligung | |
| es | Trastorno oftalmológico raro con afectación del nervio craneal | |
| it | Malattia oftalmica rara con coinvolgimento dei nervi cranici | |
| nl | Zeldzame oftalmische aandoening met betrokkenheid van hersenzenuwen | |
| pt | Doença oftalmológica rara com envolvimento dos nervos cranianos | |
| pl | Rzadka choroba oka obejmująca nerw wzrokowy | |
| cs | Vzácná oční porucha s postižením mozkového nervu | |
| uk | Рідкісне офтальмологічне захворювання з ураженням черепно-мозкових нервів | |
| zh | 伴有颅神经受累的罕见眼部疾病 | |
| tr | Kraniyal sinir tutulumu ile seyreden nadir oftalmik bozukluk |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681354 | 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:140653Neuro-ophthalmological disease
rare ophthalmic disorders
Children (7):
- ORPHA:440233Congenital abducens nerve palsy
- ORPHA:231013Congenital trigeminal anesthesia
- ORPHA:397618Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome
- ORPHA:98685Rare oculomotor nerve disorder
- ORPHA:519351Rare optic nerve disorder
- ORPHA:519353Rare trochlear nerve disorder
- ORPHA:64686Tolosa-Hunt syndrome
Codes that Orphanet moved or referred to this one:
- ORPHA:100932OBSOLETE: Nuclear oculomotor paralysis 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/519349
- This record as JSON: /data/d/519349.json