Trait
Muscle weakness between ribs
Clinical name: Intercostal muscle weakness
Lack of strength of the intercostal muscles, i.e., of the muscle groups running along the ribs that create and move the chest wall.
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page$trait$nameRead the genes linked to Muscle weakness between ribs, and the rest of your genome, with one test.
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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.
- Congenital MyopathiesReads 5 of these genesACTA1MAP3K20SELENONTPM2TPM3About this report →
- TRPV4-Related Skeletal DysplasiasReads 1 of these genesTRPV4About this report →
- Congenital Muscular DystrophiesReads 3 of these genesITGA7LAMA2SELENONAbout this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesVRK1TRPV4About this report →
Show 7 more reports
- Pontocerebellar Hypoplasia (TSEN54 and MINPP1)Reads 1 of these genesVRK1About this report →
- Spinal Muscular AtrophyReads 1 of these genesVRK1About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLAMA2About this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesVRK1TRPV4About this report →
- Hypertrophic CardiomyopathyReads 1 of these genesMYL2About this report →
- Intellectual DisabilityReads 1 of these genesVRK1About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesVRK1About this report →
Read the genes linked to Muscle weakness between ribs, and the rest of your genome, with one test.
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Get my Genome Test11 genes linked to Muscle weakness between ribs
Changes in these genes cause rare conditions in which Muscle weakness between ribs 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 |
|---|---|---|
| VRK1VRK serine/threonine kinase 1 | Often (30–79%) | In 1 condition |
| ACTA1actin alpha 1, skeletal muscle | Sometimes (5–29%) | In 1 condition |
| HACD13-hydroxyacyl-CoA dehydratase 1 | Sometimes (5–29%) | In 1 condition |
| ITGA7integrin subunit alpha 7 | Sometimes (5–29%) | In 1 condition |
| LAMA2laminin subunit alpha 2 | Sometimes (5–29%) | In 1 condition |
| MAP3K20mitogen-activated protein kinase kinase kinase 20 | Sometimes (5–29%) | In 1 condition |
| MYL2myosin light chain 2 | Sometimes (5–29%) | In 1 condition |
| SELENONselenoprotein N | Sometimes (5–29%) | In 1 condition |
| TPM2tropomyosin 2 | Sometimes (5–29%) | In 1 condition |
| TPM3tropomyosin 3 | Sometimes (5–29%) | In 1 condition |
| TRPV4transient receptor potential cation channel subfamily V member 4 | 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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