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tremor, hereditary essential, 4
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any essential tremor in which the cause of the disease is a mutation in the FUS gene.
Uniprot Description A common movement disorder mainly characterized by postural tremor of the arms. Head, legs, trunk, voice, jaw, and facial muscles also may be involved. The condition can be aggravated by emotions, hunger, fatigue and temperature extremes, and may cause a functional disability or even incapacitation. Inheritance is autosomal dominant.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0111431
OMIM:614782
UMLS:C3539195
MONDO:0013888
High level summary of knowledge for a disease, including descriptions and datasource references.