Striatal degeneration, autosomal dominant 2

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Subtype of: Striatal degeneration, autosomal dominant
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Striatal degeneration, autosomal dominant 2
MONDO_0014835
LINC00473 Unknown
27058447
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Striatal degeneration, autosomal dominant 2.
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Childhood-onset chorea with bilateral striatal lesions 1 shared geneLINC00473 Related via 1 shared gene including LINC00473. Striatal degeneration, autosomal dominant 1 shared geneLINC00473 Related via 1 shared gene including LINC00473. Dyskinesia, limb and orofacial, infantile-onset 1 shared geneLINC00473 Related via 1 shared gene including LINC00473.