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Trait

Multiple suture craniosynostosis

Craniosynostosis involving at least 2 cranial sutures, where the exact pattern of sutures fused has not been precisely specified.

HPO HP:0011324

Summary

Also called
Multisutural craniosynostosis
Body system
Abnormality of head or neckAbnormality of the musculoskeletal system

10 genes linked to Multiple suture craniosynostosis

Changes in these genes cause rare conditions in which Multiple suture 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.

GeneHow often it is seenConditions
FGFR2fibroblast growth factor receptor 2Very often (80–99%)In 1 condition
ARVCFARVCF delta catenin family memberSometimes (5–29%)In 1 condition
COMTcatechol-O-methyltransferaseSometimes (5–29%)In 1 condition
GP1BBglycoprotein Ib platelet subunit betaSometimes (5–29%)In 1 condition
HIRAhistone cell cycle regulatorSometimes (5–29%)In 1 condition
JMJD1Cjumonji domain containing 1CSometimes (5–29%)In 1 condition
RREB1ras responsive element binding protein 1Sometimes (5–29%)In 1 condition
SEC24CSEC24 homolog C, COPII componentSometimes (5–29%)In 1 condition
TBX1T-box transcription factor 1Sometimes (5–29%)In 1 condition
UFD1ubiquitin recognition factor in ER associated degradation 1Sometimes (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

Broader traits

Deformity of the skull

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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