FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term essential tremor 4 ID (Ontology) DOID:0111431 (Human Disease)
Definition An essential tremor that has_material_basis_in heterozygous mutation in FUS on chromosome 16p11.2.
Also Known As "ETM4" ; "hereditary essential tremor 4"
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DO.org
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Data Class Field Records
Human Disease Models (FBhh)  DOID       1
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 Genes Human Disease Models
 essential tremor 4       2      1
 for disease ribbon | essential tremor 4       1       --
 model of | essential tremor 4       1       --
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
movement disease                |
 |__essential tremor____________|
                                essential tremor 4  3 rec.
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Is a autosomal dominant disease
essential tremor
Part of
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Synonyms
  • "ETM4" EXACT OMO:0003012
    "hereditary essential tremor 4" EXACT
Secondary IDs
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MIM:614782