Hereditary ataxia
MONDO:0100309An instance of an atactic disorder that is caused by an inherited genomic modification in an individual.
Also known as: rare hereditary ataxia, SCA
119 clinical trials for this condition and its sub-types, 2 tagged with Hereditary ataxia itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Hereditary ataxia
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Hereditary cerebellar ataxia 0 trials · 116 incl. sub-types
5 sub-types
- Autosomal recessive cerebellar ataxia 0 trials · 72 incl. sub-types Sub-types →
- Autosomal dominant cerebellar ataxia 11 trials · 33 incl. sub-types Sub-types →
- Ataxia telangiectasia 11 trials Sub-types →
- X-linked cerebellar ataxia 0 trials Sub-types →
- Ataxia-pancytopenia syndrome 0 trials
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Spastic ataxia 1 trial · 2 incl. sub-types
6 sub-types
- Autosomal recessive spastic ataxia 0 trials · 1 incl. sub-types Sub-types →
- Autosomal dominant spastic ataxia 0 trials Sub-types →
- Spastic ataxia 10, autosomal recessive 0 trials
- Spastic ataxia 2 0 trials
- Spastic ataxia 9, autosomal recessive 0 trials
- Spasticity-ataxia-gait anomalies syndrome 0 trials
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EAST syndrome 1 trial
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Hereditary spastic paraplegia 7 1 trial
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Hereditary episodic ataxia 0 trials · 1 incl. sub-types
9 sub-types
- Episodic ataxia type 2 1 trial
- Episodic ataxia type 1 0 trials
- Episodic ataxia type 3 0 trials
- Episodic ataxia type 4 0 trials
- Episodic ataxia type 5 0 trials
- Episodic ataxia type 6 0 trials
- Episodic ataxia type 7 0 trials
- Episodic ataxia type 8 0 trials
- Episodic ataxia, type 9 0 trials
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Richards-Rundle syndrome 0 trials
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Ataxia with fasciculations 0 trials
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Autosomal dominant sensory ataxia 1 0 trials
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Cataract-ataxia-deafness syndrome 0 trials
Most studied deeper sub-types
Friedreich ataxia
(37)
Machado-Joseph disease
(11)
Marinesco-Sjogren syndrome
(10)
Spinocerebellar ataxia type 1
(10)
Spinocerebellar ataxia type 2
(10)
Spinocerebellar ataxia type 6
(9)
Spinocerebellar ataxia 7
(7)
Cerebrotendinous xanthomatosis
(6)
Cerebellar ataxia, intellectual disability, and dysequilibrium
(5)
Dentatorubral-pallidoluysian atrophy
(4)
Spinocerebellar ataxia 27B, late-onset
(4)
Spinocerebellar ataxia type 10
(4)
Spinocerebellar ataxia type 8
(4)
Abetalipoproteinemia
(2)
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome
(2)
Machado-Joseph disease type 3
(2)
Recessive mitochondrial ataxia syndrome
(2)
Spinocerebellar ataxia 9
(2)
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2
(2)
Spinocerebellar ataxia type 27
(2)