ORPHA:440233
Congenital abducens nerve palsy
Synonyms: Benign congenital sixth cranial nerve palsy · Congenital CNVI palsy
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Neonatal
- Status
- active
A rare neuro-ophthalmological disease characterized by dysfunction of the ipsilateral lateral rectus muscle with esotropia in primary position, limited or no abduction of the eyeball, and compensatory horizontal face turn toward the palsied eye. The condition commonly resolves spontaneously.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Congenital abducens nerve palsy | Benign congenital sixth cranial nerve palsy · Congenital CNVI palsy |
| fr | Paralysie congénitale du nerf abducens | Lésion CNVI congénitale · Paralysie bénigne congénitale du sixième nerf crânien |
| de | Abduzensparese, kongenitale | Benigne kongenitale Parese des sechsten Hirnnerven · Hirnnerv VI-Lähmung, kongenitale · Kongenitale Lähmung des Nervus abducens |
| es | Parálisis congénita del nervio abducens | Parálisis congénita CNVI · Parálisis congénita benigna del sexto par craneal · Parálisis congénita del nervio abducente |
| it | Paralisi congenita del nervo abducente | Paralisi congenita benigna del sesto nervo cranico · Paralisi congenita del CNVI |
| nl | Congenitale paralyse van nervus abducens | Congenitale CNVI-verlamming · Goedaardige congenitale paralyse van zesde hersenzenuw |
| pt | Paralisia congénita do nervo abducens | |
| pl | Wrodzone porażenie nerwu odwodzącego | Wrodzone łagodne porażenie szóstego nerwu czaszkowego · Wrodzone porażenie CNVI |
| cs | Vrozená paréza nervus abducens | Benigní vrozená paréza šestého hlavového nervu · Vrozená paréza n.VI |
| uk | Вроджений абдукційний нервовий параліч | Доброякісний вроджений параліч шостого черепного нерва · Вроджений CNVI параліч |
| zh | 先天性展神经麻痹 | 良性先天性第六颅神经麻痹 |
| tr | Doğumsal abdusens sinir felci | Doğumsal CNVI felci · Selim doğumsal altıncı kraniyal sinir felci |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q07.8 | NTBT | attributed | validated |
| ICD-11 | 9C81.2 | NTBT | index | validated |
| MONDO | 0018600 | E | validated | |
| UMLS | C1302994 | 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 (2):
- ORPHA:522510Rare genetic ophthalmic disorder with cranial nerve involvement
rare genetic diseases - ORPHA:519349Rare ophthalmic disorder with cranial nerve involvement
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
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/440233
- This record as JSON: /data/d/440233.json