Trait
Bowing of outer large bone of the forearm
Clinical name: Radial bowing
A bending or abnormal curvature of the radius.
Summary
- Also called
- Bowed radii, Bowed radius, Bowing of radius bone of the forearm
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Bowing of outer large bone of the forearm, and the rest of your genome, with one test.
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Get my Genome Test27 genes linked to Bowing of outer large bone of the forearm
Changes in these genes cause rare conditions in which Bowing of outer large bone of the forearm 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 |
|---|---|---|
| FGF23fibroblast growth factor 23 | Always | In 1 condition |
| FGFR3fibroblast growth factor receptor 3 | Always | In 1 condition |
| IFT43intraflagellar transport 43 | Always | In 1 condition |
| LBRlamin B receptor | Always | In 1 condition |
| TBX5T-box transcription factor 5 | Always | In 1 condition |
| TMEM67transmembrane protein 67 | Always | In 1 condition |
| SHOXSHOX homeobox | Very often (80–99%) | In 3 conditions |
| WNT7AWnt family member 7A | Very often (80–99%) | In 3 conditions |
| COL2A1collagen type II alpha 1 chain | Often (30–79%) | In 1 condition |
| GLI3GLI family zinc finger 3 | Often (30–79%) | In 1 condition |
| IHHIndian hedgehog signaling molecule | Often (30–79%) | In 1 condition |
| PRKG2protein kinase cGMP-dependent 2 | Often (30–79%) | In 1 condition |
| ROR2ROR family WNT receptor 2 | Often (30–79%) | In 1 condition |
| SLC26A2solute carrier family 26 member 2 | Sometimes (5–29%) | In 1 condition |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Sometimes (5–29%) | In 1 condition |
| B2Mbeta-2-microglobulin | Not recorded | In 1 condition |
| B3GALT6beta-1,3-galactosyltransferase 6 | Not recorded | In 1 condition |
| CCN2cellular communication network factor 2 | Not recorded | In 1 condition |
| COL11A1collagen type XI alpha 1 chain | Not recorded | In 1 condition |
| FLNAfilamin A | Not recorded | In 1 condition |
| FLNBfilamin B | Not recorded | In 2 conditions |
| GDF5growth differentiation factor 5 | Not recorded | In 1 condition |
| HOXA11homeobox A11 | Not recorded | In 1 condition |
| MMP13matrix metallopeptidase 13 | Not recorded | In 1 condition |
| NPR2natriuretic peptide receptor 2 | Not recorded | In 1 condition |
| P3H1prolyl 3-hydroxylase 1 | Not recorded | In 1 condition |
| PCNTpericentrin | 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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