Search Ontology:
Human Disease

striatal degeneration 2

Term ID
DOID:0060998
Synonyms
Definition
A multiple system atrophy characterized by hyperkinetic movements, mainly chorea, resulting from dysfunction of the basal ganglia that has_material_basis_in heterozygous mutation in the PDE10A gene on chromosome 6q27. https://pubmed.ncbi.nlm.nih.gov/27058447/
References
Ontology
Human Disease   ( DOID:0060998 )
Relationships
is a type of
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Genes Involved
Zebrafish Models