Trait
Abnormality of forearm bone
Clinical name: Abnormal forearm bone morphology
Summary
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test1 gene linked to Abnormality of forearm bone
Changes in these genes cause rare conditions in which Abnormality of forearm bone 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 |
|---|---|---|
| SLC26A2solute carrier family 26 member 2 | Sometimes (5–29%) | 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.
Narrower traits
- Abnormal morphology of ulna50 genes
- Abnormal morphology of the radius10 genes
- Bowed forearm bones2 genes
- Deformed forearm bones2 genes
- Fractured forearm bone1 gene
- Absent/small forearm bones
- Broad forearm bones
- Cortical thickening of the forearm bones
- Increased bone density of forearm bones
- Slender forearm bones
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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