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Trait
EEG with polyspike wave complexes
The presence of complexes of repetitive spikes and waves in EEG.
Summary
- Also called
- EEG: spike and multispike waves, 3-4 hz
- Body system
- Abnormality of the nervous system
EEG with polyspike wave complexesHP:0002392
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Read the genes linked to EEG with polyspike wave complexes, and the rest of your genome, with one test.
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Get my Genome Test41 genes linked to EEG with polyspike wave complexes
Changes in these genes cause rare conditions in which EEG with polyspike wave complexes 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 |
|---|---|---|
| APC2APC regulator of Wnt signaling pathway 2 | Always | In 1 condition |
| COL4A2collagen type IV alpha 2 chain | Always | In 1 condition |
| INPP4Ainositol polyphosphate-4-phosphatase type I A | Always | In 1 condition |
| CACNB4calcium voltage-gated channel auxiliary subunit beta 4 | Very often (80–99%) | In 2 conditions |
| CILK1ciliogenesis associated kinase 1 | Very often (80–99%) | In 1 condition |
| CLCN2chloride voltage-gated channel 2 | Very often (80–99%) | In 1 condition |
| CSTBcystatin B | Very often (80–99%) | In 2 conditions |
| EFHC1EF-hand domain containing 1 | Very often (80–99%) | In 2 conditions |
| GABRA1gamma-aminobutyric acid type A receptor subunit alpha1 | Very often (80–99%) | In 1 condition |
| GABRDgamma-aminobutyric acid type A receptor subunit delta | Very often (80–99%) | In 1 condition |
| JRKJrk helix-turn-helix protein | Very often (80–99%) | In 1 condition |
| KCNQ3potassium voltage-gated channel subfamily Q member 3 | Very often (80–99%) | In 1 condition |
| PRICKLE1prickle planar cell polarity protein 1 | Very often (80–99%) | In 1 condition |
| SCARB2scavenger receptor class B member 2 | Very often (80–99%) | In 1 condition |
| ADGRG1adhesion G protein-coupled receptor G1 | Often (30–79%) | In 1 condition |
| AKT3AKT serine/threonine kinase 3 | Often (30–79%) | In 1 condition |
| AP2M1adaptor related protein complex 2 subunit mu 1 | Often (30–79%) | In 2 conditions |
| CHD2chromodomain helicase DNA binding protein 2 | Often (30–79%) | In 1 condition |
| KCNC2potassium voltage-gated channel subfamily C member 2 | Often (30–79%) | In 1 condition |
| MTORmechanistic target of rapamycin kinase | Often (30–79%) | In 1 condition |
| NEXMIFneurite extension and migration factor | Often (30–79%) | In 1 condition |
| PI4KAphosphatidylinositol 4-kinase alpha | Often (30–79%) | In 1 condition |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Often (30–79%) | In 1 condition |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Often (30–79%) | In 1 condition |
| SETD1BSET domain containing 1B, histone lysine methyltransferase | Often (30–79%) | In 1 condition |
| SLC2A1solute carrier family 2 member 1 | Often (30–79%) | In 1 condition |
| SLC6A1solute carrier family 6 member 1 | Often (30–79%) | In 1 condition |
| SRPX2sushi repeat containing protein X-linked 2 | Often (30–79%) | In 1 condition |
| SYNGAP1synaptic Ras GTPase activating protein 1 | Often (30–79%) | In 1 condition |
| YEATS2YEATS domain containing 2 | Often (30–79%) | In 1 condition |
| YWHAGtyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma | Often (30–79%) | In 1 condition |
| PGAP2post-GPI attachment to proteins 2 | Sometimes (5–29%) | In 1 condition |
| PGAP3post-GPI attachment to proteins phospholipase 3 | Sometimes (5–29%) | In 1 condition |
| PIGLphosphatidylinositol glycan anchor biosynthesis class L | Sometimes (5–29%) | In 1 condition |
| PIGOphosphatidylinositol glycan anchor biosynthesis class O | Sometimes (5–29%) | In 1 condition |
| PIGVphosphatidylinositol glycan anchor biosynthesis class V | Sometimes (5–29%) | In 1 condition |
| PIGWphosphatidylinositol glycan anchor biosynthesis class W | Sometimes (5–29%) | In 1 condition |
| PIGYphosphatidylinositol glycan anchor biosynthesis class Y | Sometimes (5–29%) | In 1 condition |
| PSAT1phosphoserine aminotransferase 1 | Sometimes (5–29%) | In 1 condition |
| SPTAN1spectrin alpha, non-erythrocytic 1 | Sometimes (5–29%) | In 1 condition |
Show 1 more gene
| Gene | How often it is seen | Conditions |
|---|---|---|
| GABRG2gamma-aminobutyric acid type A receptor subunit gamma2 | 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 2026.10.16-c6eea6bf.
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