Back to discover
Disease

ATP1A3-associated neurological disorder

Also known as ATP1A3 neurological disorder, ATP1A3 related neurological disorder, neurological disorder caused by mutation in ATP1A3.

1
Associated genes
1
Related proteins

What's happening now

An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.

No activity recorded in this window. Try a wider timeframe.

Associated genes

1 match

Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.

ATP1A30.60

Disease biology

1 match

Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.

Sodium/potassium-transporting ATPase subunit alpha-3via ATP1A30.60

Reference

Authoritative identity, definition & identifiers.

Synonyms

ATP1A3 neurological disorder, ATP1A3 related neurological disorder, neurological disorder caused by mutation in ATP1A3

References & data sources
  • Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
  • Related entities are derived from literature co-mention (studied together) — associative, not causal.