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| Term | essential tremor 3 | ID (Ontology) | DOID:0111430 (Human Disease) |
| Definition | An essential tremor that has_material_basis_in variation in a region on chromosome 6p23. | ||
| Also Known As | "ETM3" ; "hereditary essential tremor 3" | ||
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| DO.org | |||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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movement disease |__essential tremor |__essential tremor 3 |
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| Is a | essential tremor | ||
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| MIM:611456 | |||