Tardive dyskinesia

Preferred Label : Tardive dyskinesia;

Type : Other, mainly phenotypes with suspected mendelian basis;

Description : Tardive dyskinesia is a debilitating motor disorder manifest as hyperkinetic, involuntary, repetitive movements predominantly of the orofacial region. It is a complication of treatment with so-called typical antipsychotic or neuroleptic agents, such as chlorpromazine or haloperidol, and is estimated to occur in 20 to 30% of chronic schizophrenics on long-term treatment (Thelma et al., 2008).;

Inheritance : Autosomal recessive predisposition;

Prefixed ID : 272620;

Details

Origin ID

272620;

UMLS CUI

C0686347;

Currated CISMeF NLP mapping
- DYSKINESIA TARDIVE [WHO-ART Preferred Term]
- Dyskinesia tardive [MedDRA LLT]
- Tardive Dyskinesia [MeSH Descriptor]
- Tardive Dyskinesia [MeSH concept]
- Tardive dyskinesia [HPO term]
- Tardive dyskinesia [MedDRA Preferred Term]
- Tardive dyskinesia (disorder) [SNOMED CT concept]
- Tardive dystonia [ICD-11 More detail]
- tardive dyskinesia [Disease (Nov.)]
- tardive dyskinesia [SNOMED Notion]
HPO term(s)
- Abnormality of the nervous system [HPO term]
- Akathisia [HPO term]
- Autosomal recessive inheritance [HPO term]
- Tardive dyskinesia [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- DYSKINESIA TARDIVE [WHO-ART Preferred Term]
- Dyskinesia tardive [MedDRA LLT]
- Tardive Dyskinesia [MeSH Descriptor]
- Tardive dyskinesia [MedDRA Preferred Term]
- Tardive dyskinesia [HPO term]
- tardive dyskinesia [SNOMED Notion]

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