Trait
EEG with generalized slow activity
Diffuse slowing of cerebral electrical activity recorded along the scalp by electroencephalography (EEG).
Summary
- Also called
- EEG with generalised slow activity, EEG: generalised slow activity, EEG: generalized slow activity
- Body system
- Abnormality of the nervous system
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to EEG with generalized slow activity, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test21 genes linked to EEG with generalized slow activity
Changes in these genes cause rare conditions in which EEG with generalized slow activity 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 |
|---|---|---|
| CDKL5cyclin dependent kinase like 5 | Always | In 1 condition |
| CYP27A1cytochrome P450 family 27 subfamily A member 1 | Always | In 1 condition |
| HID1HID1 domain containing | Very often (80–99%) | In 1 condition |
| ALDH7A1aldehyde dehydrogenase 7 family member A1 | Often (30–79%) | In 1 condition |
| CNTNAP2contactin associated protein 2 | Often (30–79%) | In 1 condition |
| MECP2methyl-CpG binding protein 2 | Often (30–79%) | In 1 condition |
| MTHFSmethenyltetrahydrofolate synthetase | Often (30–79%) | In 1 condition |
| PLPBPpyridoxal phosphate binding protein | Often (30–79%) | In 1 condition |
| RNF13ring finger protein 13 | Often (30–79%) | In 1 condition |
| AP2M1adaptor related protein complex 2 subunit mu 1 | Sometimes (5–29%) | In 1 condition |
| CHD2chromodomain helicase DNA binding protein 2 | Sometimes (5–29%) | In 1 condition |
| DOLKdolichol kinase | Sometimes (5–29%) | In 1 condition |
| DPAGT1dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | Sometimes (5–29%) | In 1 condition |
| GRIA4glutamate ionotropic receptor AMPA type subunit 4 | Sometimes (5–29%) | In 1 condition |
| KPTNkaptin, actin binding protein | Sometimes (5–29%) | In 1 condition |
| LMNB1lamin B1 | Sometimes (5–29%) | In 1 condition |
| NEXMIFneurite extension and migration factor | Sometimes (5–29%) | In 1 condition |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Sometimes (5–29%) | In 1 condition |
| SLC2A1solute carrier family 2 member 1 | Sometimes (5–29%) | In 1 condition |
| SLC6A1solute carrier family 6 member 1 | Sometimes (5–29%) | In 1 condition |
| SYNGAP1synaptic Ras GTPase activating protein 1 | Sometimes (5–29%) | 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.
Narrower traits
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 2026.10.16-c6eea6bf.
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks