Trait
Fused wrist bones
Clinical name: Carpal synostosis
Synostosis (bony fusion) involving one or more bones of the carpus (scaphoid, lunate, triquetrum, trapezium, trapezoid, capitate, hamate, pisiform).
Summary
- Also called
- Carpal bone fusion, Carpal fusion, Fused carpal bones, Fusion of carpal bones, Synostosis involving the carpal bones
This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/carpal-synostosis.json"
page <- fromJSON(url)
page$trait$nameRead the genes linked to Fused wrist bones, and the rest of your genome, with one test.
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Get my Genome Test18 genes linked to Fused wrist bones
Changes in these genes cause rare conditions in which Fused wrist bones 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 |
|---|---|---|
| BMPR1Bbone morphogenetic protein receptor type 1B | Always | In 1 condition |
| COL27A1collagen type XXVII alpha 1 chain | Always | In 1 condition |
| HOXA13homeobox A13 | Always | In 1 condition |
| NOGnoggin | Always | In 4 conditions |
| MAP3K7mitogen-activated protein kinase kinase kinase 7 | Very often (80–99%) | In 1 condition |
| FGFR3fibroblast growth factor receptor 3 | Often (30–79%) | In 1 condition |
| FLNBfilamin B | Often (30–79%) | In 2 conditions |
| MYH3myosin heavy chain 3 | Often (30–79%) | In 2 conditions |
| SALL4spalt like transcription factor 4 | Often (30–79%) | In 1 condition |
| B3GALT6beta-1,3-galactosyltransferase 6 | Sometimes (5–29%) | In 2 conditions |
| FLNAfilamin A | Sometimes (5–29%) | In 1 condition |
| CHSY1chondroitin sulfate synthase 1 | Not recorded | In 1 condition |
| GDF5growth differentiation factor 5 | Not recorded | In 1 condition |
| HOXD13homeobox D13 | Not recorded | In 1 condition |
| PAX3paired box 3 | Not recorded | In 1 condition |
| PORcytochrome p450 oxidoreductase | Not recorded | In 1 condition |
| RBM8ARNA binding motif protein 8A | Not recorded | In 1 condition |
| RECQL4RecQ like helicase 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.
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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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