Tremor, hereditary essential, 3

Preferred Label : Tremor, hereditary essential, 3;

Symbol : ETM3;

CISMeF acronym : ETM3;

Type : Phenotype or locus, molecular basis unknown;

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

Prefixed ID : %611456;

Details

Origin ID

611456;

UMLS CUI

C1969617;

Currated CISMeF NLP mapping
- tremor, hereditary essential, 3 [MeSH concept]
- tremor, hereditary essential, 3 [MeSH Supplementary Concept]
DO Cross reference
- essential tremor 3 [DO Concept]
ORDO concept(s)
- Hereditary essential tremor [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- tremor, hereditary essential, 3 [MeSH Supplementary Concept]
- tremor, hereditary essential, 3 [MeSH concept]

Keyword's position in hierarchy(ies) :

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