Trait
Decreased facial expression
A reduced degree of voluntary and involuntary facial movements involved in responded to others or expressing emotions.
Summary
- Body system
- Abnormality of head or neck
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/decreased-facial-expression.json"
page <- fromJSON(url)
page$trait$nameRead the genes linked to Decreased facial expression, and the rest of your genome, with one test.
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Get my Genome Test12 genes linked to Decreased facial expression
Changes in these genes cause rare conditions in which Decreased facial expression 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 |
|---|---|---|
| PIEZO2piezo type mechanosensitive ion channel component 2 | Always | In 1 condition |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Always | In 1 condition |
| DNA2DNA replication helicase/nuclease 2 | Often (30–79%) | In 2 conditions |
| DNMT3BDNA methyltransferase 3 beta | Often (30–79%) | In 1 condition |
| DUX4double homeobox 4 | Often (30–79%) | In 1 condition |
| DUX4L1double homeobox 4 like 1 (pseudogene) | Often (30–79%) | In 1 condition |
| FRG1FSHD region gene 1 | Often (30–79%) | In 1 condition |
| SMCHD1structural maintenance of chromosomes flexible hinge domain containing 1 | Often (30–79%) | In 1 condition |
| ASXL3ASXL transcriptional regulator 3 | Sometimes (5–29%) | In 1 condition |
| DLK1delta like non-canonical Notch ligand 1 | Sometimes (5–29%) | In 1 condition |
| MEG3maternally expressed 3 | Sometimes (5–29%) | In 1 condition |
| RTL1retrotransposon Gag like 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.
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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 2026.10.17-8666dff2.
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