Trait
Enuresis nocturna
Enuresis occurring during sleeping hours.
Summary
- Also called
- Nocturnal enuresis
- Body system
- Abnormality of the genitourinary system
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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.
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- Myofibrillar MyopathiesReads 1 of these genesKYAbout this report →
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- Osteogenesis ImperfectaReads 1 of these genesBMP1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesRNF168About this report →
- Intellectual DisabilityReads 2 of these genesZMYM3ADNPAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesFA2HAbout this report →
- Inherited Neurodegenerative DisordersReads 2 of these genesFA2HRNF168About this report →
Read the genes linked to Enuresis nocturna, and the rest of your genome, with one test.
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Get my Genome Test11 genes linked to Enuresis nocturna
Changes in these genes cause rare conditions in which Enuresis nocturna 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 |
|---|---|---|
| KYkyphoscoliosis peptidase | Always | In 1 condition |
| BMP1bone morphogenetic protein 1 | Often (30–79%) | In 1 condition |
| ZMYM3zinc finger MYM-type containing 3 | Often (30–79%) | In 1 condition |
| ADNPactivity dependent neuroprotector homeobox | Sometimes (5–29%) | In 1 condition |
| FA2Hfatty acid 2-hydroxylase | Sometimes (5–29%) | In 1 condition |
| FOXP2forkhead box P2 | Sometimes (5–29%) | In 1 condition |
| PRKAR1Bprotein kinase cAMP-dependent type I regulatory subunit beta | Sometimes (5–29%) | In 1 condition |
| RNF168ring finger protein 168 | Sometimes (5–29%) | In 1 condition |
| SLC5A2solute carrier family 5 member 2 | Sometimes (5–29%) | In 1 condition |
| AQP2aquaporin 2 | Rarely (1–4%) | In 1 condition |
| AVPR2arginine vasopressin receptor 2 | Rarely (1–4%) | 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 2026.10.19-9814e911.
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