Trait
Urethral stricture
Narrowing of the urethra associated with inflammation or scar tissue.
Summary
- Body system
- Abnormality of the genitourinary system
This page as data
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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.
- Epidermolysis BullosaReads 9 of these genesITGA6ITGB4COL7A1FERMT1LAMA3LAMB3About this report →
- Dyskeratosis CongenitaReads 2 of these genesTERTTINF2About this report →
- Familial Pulmonary FibrosisReads 1 of these genesTERTAbout this report →
- Type I InterferonopathiesReads 1 of these genesPOLA1About this report →
Show 7 more reports
- Primary Lymphoedema & Lymphatic MalformationsReads 1 of these genesFLT4About this report →
- Amelogenesis ImperfectaReads 1 of these genesLAMB3About this report →
- Bardet-Biedl and Alström SyndromesReads 1 of these genesMKKSAbout this report →
- Congenital Myasthenic SyndromeReads 1 of these genesPLECAbout this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesPLECAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesPOLA1About this report →
- Intellectual DisabilityReads 1 of these genesPOLA1About this report →
Read the genes linked to Urethral stricture, and the rest of your genome, with one test.
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Get my Genome Test17 genes linked to Urethral stricture
Changes in these genes cause rare conditions in which Urethral stricture 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 |
|---|---|---|
| ITGA6integrin subunit alpha 6 | Often (30–79%) | In 1 condition |
| ITGB4integrin subunit beta 4 | Often (30–79%) | In 1 condition |
| POLA1DNA polymerase alpha 1, catalytic subunit | Often (30–79%) | In 1 condition |
| CDC45cell division cycle 45 | Sometimes (5–29%) | In 1 condition |
| COL7A1collagen type VII alpha 1 chain | Sometimes (5–29%) | In 2 conditions |
| FERMT1FERM domain containing kindlin 1 | Sometimes (5–29%) | In 1 condition |
| FLT4fms related receptor tyrosine kinase 4 | Sometimes (5–29%) | In 1 condition |
| LAMA3laminin subunit alpha 3 | Sometimes (5–29%) | In 1 condition |
| LAMB3laminin subunit beta 3 | Sometimes (5–29%) | In 1 condition |
| LAMC2laminin subunit gamma 2 | Sometimes (5–29%) | In 1 condition |
| MKKSMKKS centrosomal shuttling protein | Sometimes (5–29%) | In 1 condition |
| MMP1matrix metallopeptidase 1 | Sometimes (5–29%) | In 1 condition |
| PKP1plakophilin 1 | Sometimes (5–29%) | In 1 condition |
| TERTtelomerase reverse transcriptase | Sometimes (5–29%) | In 1 condition |
| TINF2TERF1 interacting nuclear factor 2 | Sometimes (5–29%) | In 1 condition |
| ZMYM2zinc finger MYM-type containing 2 | Sometimes (5–29%) | In 1 condition |
| PLECplectin | 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.
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 2026.10.17-8666dff2.
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