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Primary dystonia, DYT6 type
1 OMIM reference -
1 associated gene
4 connected diseases
No signs/symptoms info
Disease Type of connection
Methylmalonic acidemia with homocystinuria, type cblX
X-linked non-syndromic intellectual deficit
Familial infantile bilateral striatal necrosis
Familial exudative vitreoretinopathy
Synonym(s):
- DYT6
- Generalized cervical and upper-limb-onset dystonia
- Idiopathic torsion dystonia of mixed type
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
THAP1 Q9NVV9609520
No signs/symptoms info available.