Trait
NREM parasomnia
A parasomnia that occurs during non-rapid eye movement (NREM) sleep.
Summary
- Also called
- Disturbance in NREM, Non-rapid eye movement parasomnia
- Body system
- Abnormality of the nervous system
Reference genomeGRCh38hg38
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Get my Genome Test15 genes linked to NREM parasomnia
Changes in these genes cause rare conditions in which NREM parasomnia 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 |
|---|---|---|
| CTSHcathepsin H | Often (30–79%) | In 1 condition |
| HCRThypocretin neuropeptide precursor | Often (30–79%) | In 1 condition |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Often (30–79%) | In 1 condition |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Often (30–79%) | In 1 condition |
| MOGmyelin oligodendrocyte glycoprotein | Often (30–79%) | In 1 condition |
| P2RY11purinergic receptor P2Y11 | Often (30–79%) | In 1 condition |
| TNFSF4TNF superfamily member 4 | Often (30–79%) | In 1 condition |
| ZNF365zinc finger protein 365 | Often (30–79%) | In 1 condition |
| CABP4calcium binding protein 4 | Rarely (1–4%) | In 1 condition |
| CHRNA2cholinergic receptor nicotinic alpha 2 subunit | Rarely (1–4%) | In 1 condition |
| CHRNA4cholinergic receptor nicotinic alpha 4 subunit | Rarely (1–4%) | In 1 condition |
| CHRNB2cholinergic receptor nicotinic beta 2 subunit | Rarely (1–4%) | In 1 condition |
| CRHcorticotropin releasing hormone | Rarely (1–4%) | In 1 condition |
| DEPDC5DEP domain containing 5, GATOR1 subcomplex subunit | Rarely (1–4%) | In 1 condition |
| KCNT1potassium sodium-activated channel subfamily T member 1 | 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.
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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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