essential tremor 2

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Summary

Literature (0)

DOID:0111429 - essential tremor 2

Disease Ontology Definition:An essential tremor that has_material_basis_in heterozygous mutation in a region on chromosome 2p25-p22.

Synonyms: ETM2, hereditary essential tremor 2,

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), essential tremor (is_a)