ATP1A3 and Movement Disease: Association Evidence

Gene-Disorder Association · Article

Gene

ATP1A3

ATPase Na+/K+ Transporting Subunit Alpha 3

Disorder

First reported 2005

Key publication · gene–disorder Genetic heterogeneity in rapid onset dystonia-parkinsonism: description of a new family.Journal of neurology, neurosurgery, and psychiatry · 2005

Key publication · disorder [The late result of surgery of extrapyramidal movement disorders and paraplegias].Deutsche Zeitschrift fur Nervenheilkunde · 1952

Manually curated

Association Review

In brief

The association between ATP1A3 (ATPase Na+/K+ Transporting Subunit Alpha 3) and Movement Disease is reported, with clinical genetic testing available.

Sources 1

Clinical variants 0

Symptoms 28

Compounds 0

Trials 0

Publications 0

At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

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Provenance

Evidence and sources

1 source

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

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ATP1A3

The gene

2 source summaries

A gene summary alongside the source descriptions it was distilled from.

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Movement Disease

The disorder

6 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

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Provenance

References & sources

4 references

Every source and publication cited across this dossier, as one numbered reference list.

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