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Disease association ontology term - MONDO:0000510 - synucleinopathy

Term summary

ID
MONDO:0000510
Name
synucleinopathy
Ontology or CV name
Disease association
Definition
A neurodegenerative disease that is characterized by the abnormal accumulation of aggregates of alpha-synuclein protein in neurons, nerve fibers or glial cells. [url:http://en.wikipedia.org/wiki/Synucleinopathies ]

Parents

Annotation

Disease association

MONDO:0010080 - familial infantile bilateral striatal necrosis

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Genes:

MONDO:0003122 - striatonigral degeneration

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Genes:

MONDO:0014889 - striatonigral degeneration, childhood-onset

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Genes:

MONDO:0010774 - striatonigral degeneration, infantile, mitochondrial

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Genes: