ORPHA:221078
Combined hyperactive dysfunction syndrome of the cranial nerves
- Type
- Disease
- Group
- Disorder
- Status
- active
A rare, acquired peripheral neuropathy characterized by symptoms arising from combined overactivity in cranial nerves, without any explanatory structural lesion. The symptoms may be unilateral or bilateral, may occur synchronously or metachronously, and include trigeminal neuralgia, hemifacial spasm and glossopharyngeal neuralgia.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Combined hyperactive dysfunction syndrome of the cranial nerves | |
| fr | Syndrome de dysfonctionnement hyperactif combiné des nerfs crâniens | |
| de | Syndrom der kombinierten hyperaktiven Dysfunktion der kranialen Nerven | |
| es | Síndrome de disfunción hiperactiva combinada de los nervios craneales | |
| it | Sindrome da disfunzione iperattiva combinata dei nervi cranici | |
| nl | Syndroom van gecombineerde hyperactieve disfunctie van hersenzenuwen | |
| pt | Síndrome de disfunção combinada hiperativa dos nervos cranianos | |
| pl | Zespół złożonej hiperaktywnej dysfunkcji nerwów czaszkowych | |
| cs | Kombinovaný syndrom hyperaktivní dysfunkce kraniálních nervů | |
| uk | Комбінований синдром гіперактивної дисфункції черепно-мозкових нервів | |
| zh | 联合颅神经多动障碍综合征 | |
| tr | Kraniyal sinirlerin kombine hiperaktif disfonksiyon sendromu |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | G52.7 | NTBT | attributed | validated |
| ICD-11 | 8A85 | NTBT | index | validated |
| MONDO | 0016371 | E | validated | |
| UMLS | C5190851 | 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:221109Cranial neuralgia
rare neurological diseases
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/221078
- This record as JSON: /data/d/221078.json