Dystonia 12
Also known as ATP1A3 dystonic disorder, DYT-ATP1A3, DYT12, dystonia type 12+5 more
ATP1A3 dystonic disorder, DYT-ATP1A3, DYT12, dystonia type 12, dystonia-12, dystonic disorder caused by mutation in ATP1A3, RDP, dystonia-Parkinsonism, rapid-onset, rapid-onset dystonia-parkinsonism.
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Associated genes
Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.
Disease biology
Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.
Reference
Authoritative identity, definition & identifiers.
ATP1A3 dystonic disorder, DYT-ATP1A3, DYT12, dystonia type 12, dystonia-12, dystonic disorder caused by mutation in ATP1A3, RDP, dystonia-Parkinsonism, rapid-onset, rapid-onset dystonia-parkinsonism
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.