Trait
Webbed 4th-5th toes
Clinical name: 4-5 toe syndactyly
Syndactyly with fusion of toes four and five.
Summary
- Also called
- Symmetric syndactyly, toes 4 and 5, Syndactyly of toes 4 and 5
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page$trait$nameRead the genes linked to Webbed 4th-5th toes, and the rest of your genome, with one test.
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Get my Genome Test12 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Feingold Syndrome Type 1Reads 1 of these genesMYCNAbout this report →
- SF3B4-Related Acrofacial Dysostosis (Nager Syndrome)Reads 1 of these genesSF3B4About this report →
- Townes-Brocks SyndromeReads 1 of these genesSALL1About this report →
- You-Hoover-Fong Syndrome (TELO2)Reads 1 of these genesTELO2About this report →
Show 8 more reports
- Meckel SyndromeReads 1 of these genesTMEM231About this report →
- Ectodermal DysplasiasReads 1 of these genesNECTIN4About this report →
- Congenital MyopathiesReads 1 of these genesMAP3K20About this report →
- Inherited IchthyosesReads 1 of these genesNSDHLAbout this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesTMEM231About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesTMEM231About this report →
- Intellectual DisabilityReads 2 of these genesNSDHLNSUN2About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesTMEM231About this report →
Read the genes linked to Webbed 4th-5th toes, and the rest of your genome, with one test.
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Get my Genome Test14 genes linked to Webbed 4th-5th toes
Changes in these genes cause rare conditions in which Webbed 4th-5th toes 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 |
|---|---|---|
| CCNQcyclin Q | Always | In 1 condition |
| NSDHLNAD(P) dependent 3-beta-hydroxysteroid dehydrogenase NSDHL | Always | In 1 condition |
| SF3B4splicing factor 3b subunit 4 | Always | In 1 condition |
| HOXD13homeobox D13 | Often (30–79%) | In 2 conditions |
| LRRC8Cleucine rich repeat containing 8 VRAC subunit C | Often (30–79%) | In 1 condition |
| MAP3K20mitogen-activated protein kinase kinase kinase 20 | Often (30–79%) | In 2 conditions |
| MYCNMYCN proto-oncogene, bHLH transcription factor | Often (30–79%) | In 2 conditions |
| NECTIN4nectin cell adhesion molecule 4 | Often (30–79%) | In 1 condition |
| NSUN2NOP2/Sun RNA methyltransferase 2 | Often (30–79%) | In 1 condition |
| TELO2telomere maintenance 2 | Often (30–79%) | In 1 condition |
| TMEM231transmembrane protein 231 | Often (30–79%) | In 1 condition |
| SALL1spalt like transcription factor 1 | Sometimes (5–29%) | In 1 condition |
| RBBP8RB binding protein 8, endonuclease | Not recorded | In 1 condition |
| TBX15T-box transcription factor 15 | 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 2026.10.19-9814e911.
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