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Disease association ontology term - MONDO:0044807 - inherited dystonia

Term summary

ID
MONDO:0044807
Name
inherited dystonia
Ontology or CV name
Disease association
Definition
An instance of dystonic disorder that is caused by an inherited modification of the individual's genome.

Parents

Annotation

Disease association

MONDO:0014557 - ataxia - oculomotor apraxia type 4

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Genes:

MONDO:0025691 - dystonia 30

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Genes:

MONDO:0030486 - dystonia 32

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Genes:

MONDO:0030513 - dystonia 33

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MONDO:0030958 - dystonia 35, childhood-onset

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MONDO:0957385 - dystonia 37, early-onset, with striatal lesions

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MONDO:0007495 - dystonia 5

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Genes:

MONDO:0015003 - dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities

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Genes:

MONDO:0000903 - myoclonus-dystonia syndrome

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MONDO:0030676 - parkinsonism-dystonia 3, childhood-onset

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Genes:

MONDO:0010334 - severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome

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MONDO:0014889 - striatonigral degeneration, childhood-onset

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MONDO:0007493 - torsion dystonia 4

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MONDO:0010747 - X-linked dystonia-parkinsonism

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