mirror movements 2
Findings
No curated finding names mirror movements 2 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 RAD51 gene.
Definition from the Mondo Disease Ontology (MONDO:0013790), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance · Typified by incomplete penetrance
- Onset and course
- Infantile onset · Childhood onset
HPO, annotations 2026-09-02
Features
1 feature
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.
- Bimanual synkinesiaHPOHP:0001335
- 10 of 18 reported patients
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.
- RAD51HGNC:9817
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2023
- Moderate · Ambry Genetics · Autosomal dominant · 2018
- Limited · G2P · Autosomal dominant · 2019
Where it sits
- A kind of
Other names
3 names
Resolves to: mirror movements 2
- Also called
- familial congenital mirror movements caused by mutation in RAD51mirror movements type 2RAD51 familial congenital mirror movements