Trait
Cardiomyocyte hypertrophy
An increase in cell size, enhanced protein synthesis, and heightened organization of the sarcomere within cardiac myocytes.
Summary
- Also called
- Myocyte cellular hypertrophy
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Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Polyglucosan Body Myopathy 2 (GYG1)Reads 1 of these genesGYG1About this report →
- Dilated CardiomyopathyReads 5 of these genesACTC1EMDTNNI3VCLDOLKAbout this report →
- Restrictive CardiomyopathyReads 1 of these genesTNNI3About this report →
- Hypertrophic CardiomyopathyReads 4 of these genesACTC1ALPK3KLHL24TNNI3About this report →
Show 8 more reports
- Epidermolysis BullosaReads 2 of these genesKLHL24DSPAbout this report →
- Syndromic and Metabolic CardiomyopathiesReads 1 of these genesACTN2About this report →
- Left Ventricular NoncompactionReads 1 of these genesACTC1About this report →
- Arrhythmogenic CardiomyopathyReads 1 of these genesDSPAbout this report →
- Inherited Congenital Heart DefectsReads 1 of these genesACTC1About this report →
- Glycogen Storage DiseaseReads 1 of these genesGYS1About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesDSPAbout this report →
- Congenital Disorders of GlycosylationReads 1 of these genesDOLKAbout this report →
Read the genes linked to Cardiomyocyte hypertrophy, and the rest of your genome, with one test.
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Get my Genome Test11 genes linked to Cardiomyocyte hypertrophy
Changes in these genes cause rare conditions in which Cardiomyocyte hypertrophy 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 |
|---|---|---|
| ACTC1actin alpha cardiac muscle 1 | Always | In 1 condition |
| ACTN2actinin alpha 2 | Always | In 1 condition |
| ALPK3alpha kinase 3 | Always | In 1 condition |
| EMDemerin | Always | In 1 condition |
| GYG1glycogenin 1 | Always | In 2 conditions |
| GYS1glycogen synthase 1 | Always | In 1 condition |
| KLHL24kelch like family member 24 | Always | In 1 condition |
| TNNI3troponin I3, cardiac type | Always | In 1 condition |
| VCLvinculin | Always | In 1 condition |
| DOLKdolichol kinase | Very often (80–99%) | In 1 condition |
| DSPdesmoplakin | 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 2026.10.19-9814e911.
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