Cobb Syndrome - CISMeF

Preferred Label : Cobb Syndrome;

NCIt synonyms : Cobb's Syndrome; Cobb s Syndrome;

NCIt definition : A rare congenital but non-hereditary disorder characterized by angiomas or arteriovenous malformations of the spinal cord. Clinical signs include sudden onset of radicular pain localizable to a dermatome with overlying cutaneous vascular lesions. Untreated, the clinical course follows a progression of sensory loss, weakness to paralysis and incontinence. However, clinical prognosis improves with endovascular embolization and/or surgical excision of the spinal lesion.;

Détails

Origin ID

C4485;

UMLS CUI

C0346068;

Currated CISMeF NLP mapping
- Cobb syndrome [ICD-11 More detail]
- Cobb syndrome [MedDRA Preferred Term]
- Cobb's syndrome (disorder) [SNOMED CT concept]
- Spinal arteriovenous metameric syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cobb syndrome [MedDRA Preferred Term]
- Cobb's syndrome (disorder) [SNOMED CT concept]
- Spinal arteriovenous metameric syndrome [ORDO Disease]
disease_has_finding
- Hereditary Lesion [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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