Inherited dystonia

MONDO:0044807

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

Also known as: familial dystonia, hereditary dystonic disorder, rare genetic dystonia, rare genetic dystonic disorder

50 clinical trials for this condition and its sub-types, 0 tagged with Inherited dystonia itself.

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Where it sits in the disease tree

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Part of

↑ Hereditary neurological disease (5772) ↑ Dystonic disorder (149)

Sub-types of Inherited dystonia

Combined dystonia 1 trial · 12 incl. sub-types
10 sub-types
- Infantile epileptic-dyskinetic encephalopathy 3 trials
- Myoclonus-dystonia syndrome 3 trials Sub-types →
- Paroxysmal dystonia 0 trials · 3 incl. sub-types Sub-types →
- Dystonia 12 2 trials
- X-linked dystonia-parkinsonism 0 trials
- Ataxia - telangiectasia variant 0 trials
- Combined cervical dystonia 0 trials
- Dystonia 16 0 trials
- Dystonia-aphonia syndrome 0 trials
- Parkinsonism-dystonia, infantile 0 trials Sub-types →
Isolated dystonia 4 trials · 11 incl. sub-types
2 sub-types
- Generalized dystonia 2 trials · 6 incl. sub-types Sub-types →
- Focal, segmental or multifocal dystonia 0 trials · 2 incl. sub-types Sub-types →
Lymphatic malformation 5 8 trials
Dystonia, focal, task-specific 4 trials
Dopa-responsive dystonia due to sepiapterin reductase deficiency 1 trial
Dystonia 28, childhood-onset 1 trial
Torsion dystonia 7 1 trial
Woodhouse-Sakati syndrome 0 trials
Ataxia - oculomotor apraxia type 4 0 trials
Autosomal dominant dopa-responsive dystonia 0 trials
2 sub-types
- Dystonia 5 0 trials
- Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism 0 trials Sub-types →
Developmental malformations-deafness-dystonia syndrome 0 trials
Dystonia 22, adult-onset 0 trials
Dystonia 22, juvenile-onset 0 trials
Dystonia 30 0 trials
Dystonia 31 0 trials
Dystonia 32 0 trials
Dystonia 33 0 trials
Dystonia 34, myoclonic 0 trials
Dystonia 35, childhood-onset 0 trials
Dystonia 37, early-onset, with striatal lesions 0 trials
Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities 0 trials
Familial idiopathic torsion dystonia 0 trials
Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome 0 trials
Striatonigral degeneration, childhood-onset 0 trials

Most studied deeper sub-types

Early-onset generalized dystonia (2) Early-onset generalized limb-onset dystonia (2) Oromandibular dystonia (2) Blepharospasm-oromandibular dystonia syndrome (1) Episodic kinesigenic dyskinesia 1 (1) Paroxysmal dyskinesia (1) Paroxysmal nonkinesigenic dyskinesia 1 (1) Adult-onset segmental dystonia (0) Benign paroxysmal torticollis of infancy (0) Brain dopamine-serotonin vesicular transport disease (0) Childhood onset GLUT1 deficiency syndrome 2 (0) Classic dopamine transporter deficiency syndrome (0) Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to a NR4A2 point mutation (0) Dystonia 21 (0) Dystonia 23 (0) Dystonia 24 (0) Dystonia 25 (0) Dystonia 27 (0) Dystonia 9 (0) ECHS1-related paroxysmal dyskinesia (0)

Including sub-types (50) Tagged with Inherited dystonia (0)

Trials to join now! 25 Not yet recruiting 3 Not yet finished but already full! 9 Completed 13

Inherited dystonia

Where it sits in the disease tree

Most studied deeper sub-types

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