inherited dystonia
MONDO:0044807Mondo
Findings
No curated finding names inherited dystonia yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An instance of dystonic disorder that is caused by an inherited modification of the individual's genome.
Definition from the Mondo Disease Ontology (MONDO:0044807), read 2026-09-29. CC BY 4.0.
Genes
3 genes
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
Where it sits
- Narrower terms (24)
- ataxia - oculomotor apraxia type 4
- autosomal dominant dopa-responsive dystonia
- combined dystonia
- developmental malformations-deafness-dystonia syndrome
- dopa-responsive dystonia due to sepiapterin reductase deficiency
- dystonia 22, adult-onset
- dystonia 22, juvenile-onset
- dystonia 28, childhood-onset
- dystonia 30
- dystonia 31
- dystonia 32
- dystonia 33
- dystonia 34, myoclonic
- dystonia 35, childhood-onset
- dystonia 37, early-onset, with striatal lesions
- dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities
- dystonia, focal, task-specific
- familial idiopathic torsion dystonia
- isolated dystonia
- lymphatic malformation 5
Other names
4 names
Resolves to: inherited dystonia
- Also called
- familial dystoniahereditary dystonic disorderrare genetic dystoniarare genetic dystonic disorder