Trait
Coronal craniosynostosis
Premature closure of the coronal suture of skull.
Summary
- Also called
- Coronal suture craniosynostosis, Coronal suture synostosis, Craniosynostosis of coronal suture
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Coronal craniosynostosis, and the rest of your genome, with one test.
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Get my Genome Test24 genes linked to Coronal craniosynostosis
Changes in these genes cause rare conditions in which Coronal craniosynostosis 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 |
|---|---|---|
| AHDC1AT-hook DNA binding motif containing 1 | Always | In 1 condition |
| FGFR2fibroblast growth factor receptor 2 | Always | In 10 conditions |
| IL11RAinterleukin 11 receptor subunit alpha | Always | In 1 condition |
| P4HBprolyl 4-hydroxylase subunit beta | Always | In 1 condition |
| RNU12RNA, U12 small nuclear | Always | In 2 conditions |
| SLC25A24solute carrier family 25 member 24 | Always | In 2 conditions |
| ALX4ALX homeobox 4 | Very often (80–99%) | In 1 condition |
| FGFR3fibroblast growth factor receptor 3 | Very often (80–99%) | In 3 conditions |
| SEC24DSEC24 homolog D, COPII component | Very often (80–99%) | In 1 condition |
| TWIST1twist family bHLH transcription factor 1 | Very often (80–99%) | In 2 conditions |
| ERFETS2 repressor factor | Often (30–79%) | In 1 condition |
| SPECC1Lsperm antigen with calponin homology and coiled-coil domains 1 like | Often (30–79%) | In 1 condition |
| BPNT23'(2'), 5'-bisphosphate nucleotidase 2 | Sometimes (5–29%) | In 1 condition |
| FGFR1fibroblast growth factor receptor 1 | Sometimes (5–29%) | In 2 conditions |
| POLA1DNA polymerase alpha 1, catalytic subunit | Sometimes (5–29%) | In 1 condition |
| RECQL4RecQ like helicase 4 | Sometimes (5–29%) | In 1 condition |
| TCOF1treacle ribosome biogenesis factor 1 | Sometimes (5–29%) | In 1 condition |
| CTSKcathepsin K | Rarely (1–4%) | In 1 condition |
| CCBE1collagen and calcium binding EGF domains 1 | Not recorded | In 1 condition |
| EFNB1ephrin B1 | Not recorded | In 1 condition |
| GTF2E2general transcription factor IIE subunit 2 | Not recorded | In 1 condition |
| MASP1MBL associated serine protease 1 | Not recorded | In 1 condition |
| PORcytochrome p450 oxidoreductase | Not recorded | In 1 condition |
| RAB23RAB23, member RAS oncogene family | 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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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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