Trait
Abnormal nervous system physiology
A functional anomaly of the nervous system.
Summary
- Also called
- Abnormality of nervous system physiology
- 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 Abnormal nervous system physiology, and the rest of your genome, with one test.
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Get my Genome Test11 genes linked to Abnormal nervous system physiology
Changes in these genes cause rare conditions in which Abnormal nervous system physiology 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 |
|---|---|---|
| DNAJC6DnaJ heat shock protein family (Hsp40) member C6 | Often (30–79%) | In 1 condition |
| PGK1phosphoglycerate kinase 1 | Often (30–79%) | In 1 condition |
| PODXLpodocalyxin like | Often (30–79%) | In 1 condition |
| SYNJ1synaptojanin 1 | Often (30–79%) | In 1 condition |
| ABCG5ATP binding cassette subfamily G member 5 | Rarely (1–4%) | In 1 condition |
| ABCG8ATP binding cassette subfamily G member 8 | Rarely (1–4%) | In 1 condition |
| APOBapolipoprotein B | Rarely (1–4%) | In 1 condition |
| GCKglucokinase | Rarely (1–4%) | In 1 condition |
| LDLRlow density lipoprotein receptor | Rarely (1–4%) | In 1 condition |
| LDLRAP1low density lipoprotein receptor adaptor protein 1 | Rarely (1–4%) | In 1 condition |
| PCSK9proprotein convertase subtilisin/kexin type 9 | 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.
Narrower traits
- Epilepsy1,808 genes
- Poor swallowing569 genes
- Headache265 genes
- Encephalopathy243 genes
- Abnormality of movement128 genes
- Tired easily98 genes
- Brain imaging abnormality72 genes
- Bulbar signs58 genes
- Somatic sensory dysfunction57 genes
- Abnormality of the sense of smell47 genes
- Abnormal central motor function46 genes
- Bulbar palsy36 genes
- Abnormal hypothalamus physiology30 genes
- Abnormality of mental function15 genes
- Neurodevelopmental abnormality15 genes
- Abnormal central sensory function12 genes
- Pseudobulbar signs11 genes
- Hypocalcemic tetany10 genes
- Abnormal cranial nerve physiology3 genes
- Abnormal nervous system electrophysiology3 genes
- Abnormal spinal cord physiology
- Abnormal synaptic transmission
- Abnormality of intracranial pressure
- Abnormality of pineal physiology
- Abnormality of taste sensation
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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