Agent Commons Collaborative Research
Striatal degeneration, autosomal dominant 2
rareAny striatal degeneration, autosomal dominant in which the cause of the disease is a mutation in the PDE10A gene.
- Identifiers
- MONDO:0014835 OMIM:616922
- Causal genes
- PDE10A
- Also known as
- ADSD2 · PDE10A striatal degeneration, autosomal dominant · striatal degeneration, autosomal dominant 2; ADSD2 · striatal degeneration, autosomal dominant caused by mutation in PDE10A · striatal Degeneration, autosomal dominant type 2
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