AtlasTrait
Disturbed sensory perception
Alteration or impairment in the processing or interpretation of sensory information can lead to abnormal perceptions or experiences.
Summary
- Also called
- Agnosia
- Body system
- Abnormality of the nervous system
AtlasThis 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/disturbed-sensory-perception.json"
page <- fromJSON(url)
page$trait$nameRead the genes linked to Disturbed sensory perception, and the rest of your genome, with one test.
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Get my Genome Test27 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Lynch SyndromeReads 5 of these genesEPCAMMLH1MSH2MSH6PMS2About this report →
- Alzheimer diseaseReads 3 of these genesTREM2APOEPSEN1About this report →
- Colorectal Cancer & PolyposisReads 3 of these genesMUTYHPOLD1POLEAbout this report →
- Adult-Onset Leukodystrophies (CSF1R, LMNB1, Nasu-Hakola)Reads 2 of these genesTREM2TYROBPAbout this report →
Show 23 more reports
- Ataxia-TelangiectasiaReads 1 of these genesATMAbout this report →
- MDPL SyndromeReads 1 of these genesPOLD1About this report →
- DNA Repair DiseaseReads 5 of these genesBRCA2MLH1MSH2MSH6PMS2About this report →
- Hereditary Breast and Ovarian Cancer (BRCA1/2)Reads 1 of these genesBRCA2About this report →
- Hereditary Mixed Polyposis SyndromeReads 1 of these genesBMPR1AAbout this report →
- Juvenile Polyposis SyndromeReads 1 of these genesBMPR1AAbout this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 2 of these genesATMCHEK2About this report →
- MTOR Pathway Megalencephaly and Overgrowth DisordersReads 1 of these genesPIK3CAAbout this report →
- Loeys-Dietz SyndromeReads 1 of these genesTGFBR2About this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesKRASAbout this report →
- Marfan Like SyndromesReads 1 of these genesTGFBR2About this report →
- Aortic AneurysmReads 1 of these genesTGFBR2About this report →
- Congenital Diarrhoeas & EnteropathiesReads 1 of these genesEPCAMAbout this report →
- Frontotemporal DementiaReads 1 of these genesPSEN1About this report →
- HyperlipidemiaReads 1 of these genesAPOEAbout this report →
- Inherited Neurodegenerative DisordersReads 5 of these genesTREM2TYROBPAPOEATMPSEN1About this report →
- Fanconi AnemiaReads 1 of these genesBRCA2About this report →
- Other Inherited LeukodystrophiesReads 2 of these genesTREM2TYROBPAbout this report →
- Autoimmune DiseaseReads 1 of these genesKRASAbout this report →
- Noonan SyndromeReads 1 of these genesKRASAbout this report →
- Other Inborn Errors of ImmunityReads 3 of these genesATMKRASPOLD1About this report →
- Female InfertilityReads 1 of these genesATMAbout this report →
- Hypertrophic CardiomyopathyReads 1 of these genesKRASAbout this report →
Read the genes linked to Disturbed sensory perception, and the rest of your genome, with one test.
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Get my Genome Test23 genes linked to Disturbed sensory perception
Changes in these genes cause rare conditions in which Disturbed sensory perception 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 |
|---|---|---|
| TREM2triggering receptor expressed on myeloid cells 2 | Often (30–79%) | In 3 conditions |
| TYROBPtransmembrane immune signaling adaptor TYROBP | Often (30–79%) | In 2 conditions |
| APOEapolipoprotein E | Sometimes (5–29%) | In 1 condition |
| ATMATM serine/threonine kinase | Sometimes (5–29%) | In 1 condition |
| BMPR1Abone morphogenetic protein receptor type 1A | Sometimes (5–29%) | In 1 condition |
| BRCA2BRCA2 DNA repair associated | Sometimes (5–29%) | In 1 condition |
| CHEK2checkpoint kinase 2 | Sometimes (5–29%) | In 1 condition |
| EPCAMepithelial cell adhesion molecule | Sometimes (5–29%) | In 1 condition |
| KRASKRas proto-oncogene, GTPase | Sometimes (5–29%) | In 1 condition |
| MLH1mutL homolog 1 | Sometimes (5–29%) | In 1 condition |
| MSH2mutS homolog 2 | Sometimes (5–29%) | In 1 condition |
| MSH6mutS homolog 6 | Sometimes (5–29%) | In 1 condition |
| MUTYHmutY DNA glycosylase | Sometimes (5–29%) | In 1 condition |
| NPATnuclear protein, coactivator of histone transcription | Sometimes (5–29%) | In 1 condition |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Sometimes (5–29%) | In 1 condition |
| PMS1PMS1 homolog 1, mismatch repair system component | Sometimes (5–29%) | In 1 condition |
| PMS2PMS1 homolog 2, mismatch repair system component | Sometimes (5–29%) | In 1 condition |
| POLD1DNA polymerase delta 1, catalytic subunit | Sometimes (5–29%) | In 1 condition |
| POLEDNA polymerase epsilon, catalytic subunit | Sometimes (5–29%) | In 1 condition |
| PSEN1presenilin 1 | Sometimes (5–29%) | In 1 condition |
| RPS20ribosomal protein S20 | Sometimes (5–29%) | In 1 condition |
| SEMA4Asemaphorin 4A | Sometimes (5–29%) | In 1 condition |
| TGFBR2transforming growth factor beta receptor 2 | 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.
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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 2026.10.19-9814e911.
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