Trait
Holes in parietal bones
Clinical name: Parietal foramina
The presence of symmetrical and circular openings (foramina) in the parietal bone ranging in size from a few millimeters to several centimeters wide.
Summary
- Also called
- Openings in parietal bones, Persistent foramina of the parietal bones, Symmetrical, oval defects in the parietal bone, Symmetrical, oval parietal bone defects
Read the genes linked to Holes in parietal bones, and the rest of your genome, with one test.
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Get my Genome Test14 genes linked to Holes in parietal bones
Changes in these genes cause rare conditions in which Holes in parietal 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 |
|---|---|---|
| ALX4ALX homeobox 4 | Always | In 4 conditions |
| MSX2msh homeobox 2 | Always | In 3 conditions |
| RNU12RNA, U12 small nuclear | Always | In 2 conditions |
| EXT2exostosin glycosyltransferase 2 | Often (30–79%) | In 1 condition |
| PHF21APHD finger protein 21A | Often (30–79%) | In 1 condition |
| ZSWIM6zinc finger SWIM-type containing 6 | Often (30–79%) | In 1 condition |
| FGFR2fibroblast growth factor receptor 2 | Sometimes (5–29%) | In 2 conditions |
| FGFR3fibroblast growth factor receptor 3 | Sometimes (5–29%) | In 1 condition |
| PPM1Dprotein phosphatase, Mg2+/Mn2+ dependent 1D | Sometimes (5–29%) | In 1 condition |
| TWIST1twist family bHLH transcription factor 1 | Sometimes (5–29%) | In 2 conditions |
| ZIC1Zic family zinc finger 1 | Sometimes (5–29%) | In 1 condition |
| CREBBPCREB binding lysine acetyltransferase | Not recorded | In 1 condition |
| EP300EP300 lysine acetyltransferase | Not recorded | In 1 condition |
| RPS19ribosomal protein S19 | 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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