Congenital cervical spinal stenosis
Synonyms: Congenital narrowing of cervical spinal canal · Congenital stenosis of the cervical spine
- Type
- Disease
- Group
- Disorder
- Age of onset
- Adolescent, Adult
- Status
- active
Congenital cervical spinal stenosis is a rare neurological disease characterized by a congenital narrowing of the bony anatomy of the cervical spinal canal (saggital diameter <14mm), predisposing the individual to symptomatic neural compression, such as cramps, paresthesias, pain, muscle hypertonia and weakness, myelopathy and sphincter disturbances.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Congenital cervical spinal stenosis | Congenital narrowing of cervical spinal canal · Congenital stenosis of the cervical spine |
| fr | Sténose spinale cervicale congénitale | Rétrecissement congénital du canal médullaire cervical |
| de | Zervikale Spinalkanalstenose, kongenitale | Stenose der Halswirbelsäule, kongenitale · Zervikale Spinalstenose, kongenitale |
| es | Estenosis espinal cervical congénita | Estenosis congénita de la columna cervical · Estrechamiento congénito del canal espinal cervical |
| it | Stenosi congenita del canale spinale cervicale | |
| nl | Congenitale cervicale spinale stenose | Congenitale stenose van de cervicale wervelkolom · Congenitale vernauwing van het cervicale wervelkanaal |
| pt | Estenose do canal medular cervical congénita | |
| pl | Wrodzone zwężenie kanału rdzeniowego kręgowego w odcinku szyjnym | = en |
| cs | Vrozené zúžení cervikální části páteřního kanálu | = en |
| uk | Вроджений стеноз шийного відділу хребта | Вроджене звуження шийного відділу хребетного каналу · Вроджений стеноз шийного відділу хребта |
| zh | 先天性颈椎管狭窄 | 先天性颈椎管狭窄症 |
| tr | Doğumsal servikal spinal stenoz | Servikal omurganın Doğumsal stenozu · Doğumsal servikal spinal kanalın daralması |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q06.8 | NTBT | attributed | validated |
| MONDO | 0019357 | E | validated | |
| UMLS | C4749275 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:102000Medullar disease
rare neurological diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/831
- This record as JSON: /data/d/831.json