mirror movements 3
Findings
No curated finding names mirror movements 3 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any familial congenital mirror movements in which the cause of the disease is a mutation in the DNAL4 gene.
Definition from the Mondo Disease Ontology (MONDO:0014478), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal recessive inheritance
HPO, annotations 2026-09-02
Features
2 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Situs inversus totalisHPOHP:0001696
- 0 of 3 reported patients
- Bimanual synkinesiaHPOHP:0001335
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.
- DNAL4HGNC:2955
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2018
Where it sits
- A kind of
Other names
3 names
Resolves to: mirror movements 3
- Also called
- DNAL4 familial congenital mirror movementsfamilial congenital mirror movements caused by mutation in DNAL4mirror movements type 3