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GTR Home > Conditions/Phenotypes > Tremor, hereditary essential, 5

Tremor, hereditary essential, 5

Summary

Hereditary essential tremor-5 (ETM5) is an autosomal dominant neurologic disorder characterized by kinetic, intention, and/or postural tremor mainly affecting the upper limbs. The age at onset and severity are highly variable, even within families (summary by Hor et al., 2015). For a general phenotypic description and a discussion of genetic heterogeneity of hereditary essential tremor, see ETM1 (190300). [from OMIM]

Available tests

7 tests are in the database for this condition.

Clinical tests (7 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: Doc4, ETM5, ODZ4, TEN4, TNM4, Ten-M4, ten-4, TENM4
    Summary: teneurin transmembrane protein 4

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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