Trait
Abnormality of shape of baby molar
Clinical name: Abnormal primary molar morphology
An abnormality of morphology of primary molar.
Summary
- Also called
- Abnormality of deciduous molar morphology, Abnormality of primary molar morphology, Abnormality of shape of primary molar
- Body system
- Abnormality of head or neck
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Abnormality of shape of baby molar, and the rest of your genome, with one test.
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Get my Genome Test13 genes linked to Abnormality of shape of baby molar
Changes in these genes cause rare conditions in which Abnormality of shape of baby molar 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 |
|---|---|---|
| EDAectodysplasin A | Sometimes (5–29%) | In 1 condition |
| EDARADDEDAR associated via death domain | Sometimes (5–29%) | In 1 condition |
| FGFR1fibroblast growth factor receptor 1 | Sometimes (5–29%) | In 1 condition |
| GREM2gremlin 2, DAN family BMP antagonist | Sometimes (5–29%) | In 1 condition |
| IRF6interferon regulatory factor 6 | Sometimes (5–29%) | In 1 condition |
| LRP6LDL receptor related protein 6 | Sometimes (5–29%) | In 1 condition |
| MSX1msh homeobox 1 | Sometimes (5–29%) | In 1 condition |
| PAX9paired box 9 | Sometimes (5–29%) | In 1 condition |
| SMARCAL1SNF2 related chromatin remodeling annealing helicase 1 | Sometimes (5–29%) | In 1 condition |
| SUMO1small ubiquitin like modifier 1 | Sometimes (5–29%) | In 1 condition |
| TGFAtransforming growth factor alpha | Sometimes (5–29%) | In 1 condition |
| WNT10AWnt family member 10A | Sometimes (5–29%) | In 1 condition |
| WNT10BWnt family member 10B | Sometimes (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.
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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