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Disease association ontology term - MONDO:0003996 - basal ganglia disorder

Term summary

ID
MONDO:0003996
Name
basal ganglia disorder
Ontology or CV name
Disease association
Definition
A disease involving the basal ganglia.

Parents

Annotation

Disease association

MONDO:0014796 - autosomal recessive early-onset Parkinson disease 23

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MONDO:0011658 - autosomal recessive early-onset Parkinson disease 7

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MONDO:0980939 - basal ganglia calcification, idiopathic, 11, autosomal recessive

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MONDO:0014628 - basal ganglia calcification, idiopathic, 6

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MONDO:0008947 - bilateral striopallidodentate calcinosis

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MONDO:0014233 - early-onset Parkinson disease 20

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MONDO:0011706 - Kufor-Rakeb syndrome

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MONDO:0008199 - late-onset Parkinson disease

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MONDO:0005180 - Parkinson disease

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MONDO:0013625 - Parkinson disease 17

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MONDO:0014742 - Parkinson disease 22, autosomal dominant

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MONDO:0957576 - Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development

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

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MONDO:0008201 - Perry syndrome

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MONDO:0010747 - X-linked dystonia-parkinsonism

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