TREMOR, HEREDITARY ESSENTIAL, 2

General Information (adopted from Orphanet):

Synonyms, Signs: ETM2
Number of Symptoms 4
OrphanetNr:
OMIM Id: 602134
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal dominant inheritance
[Omim]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
 (HPO:0007351) Upper limb postural tremor 2 / 7739
2
 (OMIM) Variable tremor of head, legs, trunk, voice, jaw, and facial muscles 1 / 7739
3
 (MedDRA:10015496) Essential tremor 4 / 7739
4
 (HPO:0000006) Autosomal dominant inheritance 2518 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information:

Molecular genetics OMIM Although Higgins et al. (2005) reported an association between essential tremor and a substitution in the HS1BP3 gene (609359), Deng et al. (2005) found no association between the same substitution and essential tremor or Parkinson disease (168600) among ...