Other specified extrapyramidal and movement disorders

Preferred Label : Other specified extrapyramidal and movement disorders;

Diag associé à un acte (%) : 84.3;

CMA : 2;

Source : OMS;

Date de début : 01/01/1997;

Date de mise à jour : 01/01/2018;

Details

Origin ID

G258;

UMLS CUI

C0477362;

DO Cross reference
- hyperekplexia [DO Concept]
- hyperekplexia 1 [DO Concept]
- hyperekplexia 2 [DO Concept]
- hyperekplexia 3 [DO Concept]
Excluded by
- Other disorders of muscle [ICD-10 category]
Orphanet concepts
- Brain dopamine-serotonin vesicular transport disease [ORDO Disease]
- Classic stiff person syndrome [ORDO Disease]
- Familial congenital mirror movements [ORDO Disease]
- Focal stiff limb syndrome [ORDO Disease]
- Hereditary hyperekplexia [ORDO Disease]
- Hyperekplexia [ORDO Disease]
- Hyperekplexia-epilepsy syndrome [ORDO Disease]
- Sporadic hyperekplexia [ORDO Disease]
- Stiff person spectrum disorder [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Other Specified Extrapyramidal and Movement Disorders [NCIt concept]
Validated automatic mappings to BTNT
- hyperekplexia 3 [DO Concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients