Genopathy
Gene-Disorder Association · Article
Gene
DYT15
Dystonia 15, Myoclonic
Disorder
Dystonia 11, Myoclonic
First reported 1953
Key publication · disorder Nocturnal myoclonus.Journal of neurology, neurosurgery, and psychiatry · 1953
Manually curated
Association Review

In brief

The association between DYT15 (Dystonia 15, Myoclonic) and Dystonia 11, Myoclonic is a manually-curated gene–disease association, supported by a single expert-curated source.

Sources 1
Clinical variants 0
Symptoms 28
Compounds 0
Trials 0
Publications 0
01
At a glance

Association overview

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

Request access
02
Provenance

Evidence and sources

1 source

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

Request access
03
Dystonia 11, Myoclonic

The disorder

13 database identifiers

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

Request access
04
Phenotype

Clinical features

22 clinical features

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

Request access
05
Provenance

References & sources

4 references

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

Request access