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1.

Striatal degeneration, autosomal dominant 2

Autosomal dominant striatal degeneration-2 is a neurologic disorder characterized by hyperkinetic movements, mainly chorea, resulting from dysfunction of the basal ganglia. Although symptoms appear in the first decade, the disorder is not progressive (summary by Mencacci et al., 2016). For a discussion of genetic heterogeneity of ADSD, see ADSD1 (609161). [from OMIM]

MedGen UID:
934758
Concept ID:
C4310791
Disease or Syndrome
2.

Abnormal corpus striatum morphology

Abnormality of the striatum, which is the largest nucleus of the basal ganglia, comprising the caudate, putamen and ventral striatum, including the nucleus accumbens. [from HPO]

MedGen UID:
869185
Concept ID:
C4023607
Anatomical Abnormality

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