Other dystonia

Preferred Label : Other dystonia;

Inclusion CIM-10 : Acquired torsion dystonia NOS;

Diag associé à un acte (%) : 82.2;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

G248;

UMLS CUI

C0477360;

DO Cross reference
- childhood onset GLUT1 deficiency syndrome 2 [DO Concept]
- dystonia 23 [DO Concept]
- dystonia 24 [DO Concept]
- dystonia 9 [DO Concept]
- episodic kinesigenic dyskinesia 1 [DO Concept]
- episodic kinesigenic dyskinesia 2 [DO Concept]
- paroxysmal nonkinesigenic dyskinesia 1 [DO Concept]
- paroxysmal nonkinesigenic dyskinesia 2 [DO Concept]
Orphanet concepts
- Adult-onset cervical dystonia, DYT23 type [ORDO Disease]
- Aromatic L-amino acid decarboxylase deficiency [ORDO Disease]
- Blepharospasm-oromandibular dystonia syndrome [ORDO Disease]
- Cranio-cervical dystonia with laryngeal and upper-limb involvement [ORDO Disease]
- Dopa-responsive dystonia [ORDO Disease]
- Dystonia 28 [ORDO Disease]
- Dystonia-aphonia syndrome [ORDO Disease]
- Focal, segmental or multifocal dystonia [ORDO Disease]
- Hemidystonia-hemiatrophy syndrome [ORDO Disease]
- Infantile dystonia-parkinsonism [ORDO Disease]
- Infantile-onset generalized dyskinesia with orofacial involvement [ORDO Disease]
- Limb dystonia [ORDO Disease]
- Paroxysmal dyskinesia [ORDO Disease]
- Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity [ORDO Disease]
- Paroxysmal exertion-induced dyskinesia [ORDO Disease]
- Paroxysmal hypnogenic dyskinesia [ORDO Disease]
- Paroxysmal kinesigenic dyskinesia [ORDO Disease]
- Paroxysmal non-kinesigenic dyskinesia [ORDO Disease]
- Sandifer syndrome [ORDO Disease]
- Truncal dystonia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Other Dystonia [NCIt concept]
Validated automatic mappings to BTNT
- childhood onset GLUT1 deficiency syndrome 2 [DO Concept]

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