Trait
Abnormality of mental function
Cognitive, psychiatric, or memory anomaly.
Summary
- Also called
- Abnormality of higher mental function
- Body system
- Abnormality of the nervous system
This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/abnormality-of-mental-function.json"
page <- fromJSON(url)
page$trait$nameRead the genes linked to Abnormality of mental function, and the rest of your genome, with one test.
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Get my Genome Test15 genes linked to Abnormality of mental function
Changes in these genes cause rare conditions in which Abnormality of mental function 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 |
|---|---|---|
| ACAT1acetyl-CoA acetyltransferase 1 | Very often (80–99%) | In 1 condition |
| ATP13A2ATPase cation transporting 13A2 | Often (30–79%) | In 1 condition |
| SPG7SPG7 matrix AAA peptidase subunit, paraplegin | Often (30–79%) | In 1 condition |
| APPamyloid beta precursor protein | Sometimes (5–29%) | In 1 condition |
| GALTgalactose-1-phosphate uridylyltransferase | Sometimes (5–29%) | In 1 condition |
| MEN1menin 1 | Sometimes (5–29%) | In 1 condition |
| PRNPprion protein (Kanno blood group) | Sometimes (5–29%) | In 1 condition |
| PSEN1presenilin 1 | Sometimes (5–29%) | In 1 condition |
| PSEN2presenilin 2 | Sometimes (5–29%) | In 1 condition |
| REEP2receptor accessory protein 2 | Sometimes (5–29%) | In 1 condition |
| SORL1sortilin related receptor 1 | Sometimes (5–29%) | In 1 condition |
| TOMM40translocase of outer mitochondrial membrane 40 | Sometimes (5–29%) | In 1 condition |
| TREM2triggering receptor expressed on myeloid cells 2 | Sometimes (5–29%) | In 1 condition |
| YY1YY1 transcription factor | Sometimes (5–29%) | In 1 condition |
| CRPPACDP-L-ribitol pyrophosphorylase A | 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
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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