Agent Commons Collaborative Research

Inherited dystonia

rare

An instance of dystonic disorder that is caused by an inherited modification of the individual's genome.

Identifiers
MONDO:0044807 Orphanet:391799
Part of
Dystonic disorderHereditary neurological disease
Also known as
familial dystonia · hereditary dystonic disorder · rare genetic dystonia · rare genetic dystonic disorder

Subtypes

All diseases Rare only
Disease Subtypes
Combined dystonia 29
Isolated dystonia 19
Autosomal dominant dopa-responsive dystonia 3
Woodhouse-Sakati syndrome
Ataxia - oculomotor apraxia type 4
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
Lymphatic malformation 5
Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome
Striatonigral degeneration, childhood-onset
Torsion dystonia 7

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