mirror movements 1
MONDO:0008002Mondo
Findings
No curated finding names mirror movements 1 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 DCC gene.
Definition from the Mondo Disease Ontology (MONDO:0008002), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance · Typified by incomplete penetrance
- Onset and course
- Infantile onset
HPO, annotations 2026-09-02
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.
- DCCHGNC:2701
- Definitive · Illumina · Autosomal dominant · 2018
- Strong · Ambry Genetics · Autosomal dominant · 2017
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2023
- Strong · PanelApp Australia · Autosomal dominant · 2025
Where it sits
Other names
3 names
Resolves to: mirror movements 1
- Also called
- DCC familial congenital mirror movementsfamilial congenital mirror movements caused by mutation in DCCmirror movements type 1