Tremor, hereditary essential, 2

Preferred Label : Tremor, hereditary essential, 2;

Symbol : ETM2;

CISMeF acronym : ETM2;

Type : Phenotype or locus, molecular basis unknown;

Description : For a phenotypic description and a discussion of genetic heterogeneity of essential tremor, see ETM1 (190300).;

Inheritance : Autosomal dominant;

Prefixed ID : %602134;

Details

Origin ID

602134;

UMLS CUI

C1865810;

Broader ORDO disease(s)
- Hereditary essential tremor [ORDO Disease]
DO Cross reference
- essential tremor 2 [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Fatigue [HPO term]
- Kinetic tremor [HPO term]
- Postural tremor of arms [HPO term]
- Upper limb postural tremor [HPO term]
ORDO concept(s)
- Hereditary essential tremor [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Tremor hereditary essential, 2 [MeSH concept]
- tremor hereditary essential, 2 [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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