Trait
Oligodactyly
A developmental defect resulting in the presence of fewer than the normal number of digits.
Summary
Reference genomeGRCh38hg38
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Get my Genome Test28 genes linked to Oligodactyly
Changes in these genes cause rare conditions in which Oligodactyly 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 |
|---|---|---|
| FAAP100FA core complex associated protein 100 | Always | In 1 condition |
| RIPK4receptor interacting serine/threonine kinase 4 | Always | In 1 condition |
| APCAPC regulator of Wnt signaling pathway | Very often (80–99%) | In 1 condition |
| BTRCbeta-transducin repeat containing E3 ubiquitin protein ligase | Very often (80–99%) | In 1 condition |
| DLX5distal-less homeobox 5 | Very often (80–99%) | In 1 condition |
| DLX6distal-less homeobox 6 | Very often (80–99%) | In 1 condition |
| EPS15L1epidermal growth factor receptor pathway substrate 15 like 1 | Very often (80–99%) | In 1 condition |
| FBXW4F-box and WD repeat domain containing 4 | Very often (80–99%) | In 1 condition |
| LRP4LDL receptor related protein 4 | Very often (80–99%) | In 1 condition |
| SEM1SEM1 26S proteasome subunit | Very often (80–99%) | In 1 condition |
| TP63tumor protein p63 | Very often (80–99%) | In 3 conditions |
| WNT10BWnt family member 10B | Very often (80–99%) | In 1 condition |
| H4C3H4 clustered histone 3 | Often (30–79%) | In 1 condition |
| RECQL4RecQ like helicase 4 | Often (30–79%) | In 1 condition |
| BRD4bromodomain containing 4 | Sometimes (5–29%) | In 1 condition |
| GLI3GLI family zinc finger 3 | Sometimes (5–29%) | In 3 conditions |
| HDAC8histone deacetylase 8 | Sometimes (5–29%) | In 1 condition |
| MAU2MAU2 sister chromatid cohesion factor | Sometimes (5–29%) | In 1 condition |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Sometimes (5–29%) | In 1 condition |
| NIPBLNIPBL cohesin loading factor | Sometimes (5–29%) | In 2 conditions |
| NSDHLNAD(P) dependent 3-beta-hydroxysteroid dehydrogenase NSDHL | Sometimes (5–29%) | In 1 condition |
| RAD21RAD21 cohesin complex component | Sometimes (5–29%) | In 1 condition |
| SMC1Astructural maintenance of chromosomes 1A | Sometimes (5–29%) | In 1 condition |
| SMC3structural maintenance of chromosomes 3 | Sometimes (5–29%) | In 1 condition |
| CYP26B1cytochrome P450 family 26 subfamily B member 1 | Not recorded | In 1 condition |
| DONSONDNA replication fork stabilization factor DONSON | Not recorded | In 1 condition |
| HOXD13homeobox D13 | Not recorded | In 1 condition |
| WNT7AWnt family member 7A | 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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