ATP1A3-associated neurological disorder
MONDO:0700002Mondo
Findings
No curated finding names ATP1A3-associated neurological disorder yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any neurological disorder in which the cause of the disease is a mutation in the ATP1A3.
Definition from the Mondo Disease Ontology (MONDO:0700002), read 2026-09-29. CC BY 4.0.
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- ATP1A3HGNC:801
- Definitive · ClinGen · Autosomal dominant · 2022
- Definitive · Illumina · Autosomal dominant · 2020
- Strong · PanelApp Australia · Autosomal dominant · 2025
Where it sits
- A kind of
Other names
3 names
Resolves to: ATP1A3-associated neurological disorder
- Also called
- ATP1A3 neurological disorderATP1A3 related neurological disorderneurological disorder caused by mutation in ATP1A3