Geniospasm 1 - CISMeF

Preferred Label : Geniospasm 1;

Symbol : GSM1;

CISMeF acronym : GSM1;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Trembling chin;

Description : Geniospasm is characterized by spontaneous intermittent involuntary quivering or trembling of the chin that is intensified by stress or anxiety. The movements are first noticed in infancy or childhood and usually abate by late adulthood (Wadlington, 1958; Danek et al., 1991).;

Inheritance : Autosomal dominant;

Prefixed ID : %190100;

Details

Origin ID

190100;

UMLS CUI

C1860972;

Currated CISMeF NLP mapping
- Hereditary geniospasm [ORDO Disease]
- Hereditary geniospasm [MeSH concept]
- Hereditary geniospasm (disorder) [SNOMED CT concept]
HPO term(s)
- Anxiety [HPO term]
- Autosomal dominant inheritance [HPO term]
- Chin myoclonus [HPO term]
ORDO concept(s)
- Hereditary geniospasm [ORDO Disease]
Semantic type(s)
- Finding [UMLS semantic type]
UMLS correspondences (same concept)
- Chin myoclonus [HPO term]
- Geniospasm [MedDRA Preferred Term]
- geniospasm [MeSH Supplementary Concept]
- geniospasm [MeSH concept]
Validated automatic mappings to NTBT
- geniospasm [MeSH concept]

Keyword's position in hierarchy(ies) :

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