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Disease association ontology term - MONDO:0003122 - striatonigral degeneration

Term summary

ID
MONDO:0003122
Name
striatonigral degeneration
Ontology or CV name
Disease association
Definition
A progressive neurodegenerative disorder caused by a disruption in the connection between the striatum and the substantia nigra. It is a type of multiple system atrophy (MSA). Signs and symptoms include rigidity, instability, impaired speech, and slow movements.

Parents

Annotation

Disease association

MONDO:0003122 - striatonigral degeneration

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MONDO:0010080 - familial infantile bilateral striatal necrosis

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MONDO:0014889 - striatonigral degeneration, childhood-onset

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MONDO:0010774 - striatonigral degeneration, infantile, mitochondrial

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