Trait
Myofiber disarray
A nonparallel arrangement of cardiac myocytes.
Summary
- Also called
- Myocardial fiber disarray, Myocardial fibre disarray
- Body system
- Abnormality of the cardiovascular system
Reference genomeGRCh38hg38
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Get my Genome Test10 genes linked to Myofiber disarray
Changes in these genes cause rare conditions in which Myofiber disarray is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| LMOD2leiomodin 2 | Always | In 1 condition |
| MYBPC3myosin binding protein C3 | Always | In 1 condition |
| MYL2myosin light chain 2 | Always | In 1 condition |
| VCLvinculin | Always | In 1 condition |
| ACTN2actinin alpha 2 | Often (30–79%) | In 1 condition |
| PPP1R13Lprotein phosphatase 1 regulatory subunit 13 like | Often (30–79%) | In 1 condition |
| SCO2synthesis of cytochrome C oxidase 2 | Often (30–79%) | In 1 condition |
| SMPXsmall muscle protein X-linked | Often (30–79%) | In 1 condition |
| TPM2tropomyosin 2 | Sometimes (5–29%) | In 1 condition |
| PRKAG2protein kinase AMP-activated non-catalytic subunit gamma 2 | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
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