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Striatal Degeneration 2

Disease ID: disease_node_16123

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Dbxref	MIM:616922
Subclassof	DOID_0050736, DOID_4752
Data Source	DOID
Doid Label	striatal degeneration 2
Doid Description	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.
Has Material Basis In	GENO_0000147
Disease Node Id	disease_node_16123
Doid Id	DOID_0060998
Label	Striatal Degeneration 2

Outgoing r'ship SUBCLASS_OF to/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Shy-Drager Syndrome(ID:disease_node_6908) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Multiple System Atrophy(ID:disease_node_9976) (Disease)

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