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Autosomal dominant cervical dystonia
3 OMIM references -
2 associated genes
4 connected diseases
No signs/symptoms info
Disease Type of connection
Benign essential blepharospasm
Childhood absence epilepsy
Dravet syndrome
Generalized epilepsy with febrile seizures-plus context
- Autosomal dominant spasmodic torticollis

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: normal
Type of inheritance: autosomal dominant
External references:
3 OMIM references -
No MeSH references

Gene symbol UniProt reference OMIM reference
ANO3 Q9BYT9610110
DRD5 P21918126453
No signs/symptoms info available.