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Metadata
ID	DOID:0060998
Name	striatal degeneration 2
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/
Xrefs	MIM:616922
Parent Relationships	is_a autosomal dominant disease is_a multiple system atrophy
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance