Trait
Cleft lower jaw
Clinical name: Cleft mandible
Midline deficiency of the mandible and some or all overlying tissues.
Summary
- Also called
- Mandibular cleft
Reference genomeGRCh38hg38
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Get my Genome Test1 gene linked to Cleft lower jaw
Changes in these genes cause rare conditions in which Cleft lower jaw 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 |
|---|---|---|
| EIF4A3eukaryotic translation initiation factor 4A3 | Very often (80–99%) | In 2 conditions |
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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