Striatal degeneration, autosomal dominant 2

Definition

Any striatal degeneration, autosomal dominant in which the cause of the disease is a mutation in the PDE10A gene.

Also known as ADSD2, PDE10A striatal degeneration, autosomal dominant, striatal Degeneration, autosomal dominant 2, striatal degeneration, autosomal dominant 2; ADSD2, striatal degeneration, autosomal dominant caused by mutation in PDE10A, striatal Degeneration, autosomal dominant type 2 — per MONDO

Also identified as

• DOID 0060998 per MONDO
• OMIM 616922 per MONDO
• UMLS C4310791 per MONDO