Trait

Low APGAR score

Body system: Abnormality of prenatal development or birth

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/low-apgar-score.json"
page <- fromJSON(url)
page$trait$name

Open the JSON

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6 genes linked to Low APGAR score

Changes in these genes cause rare conditions in which Low APGAR score 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
MTM1myotubularin 1	Very often (80–99%)	In 1 condition
ALDH7A1aldehyde dehydrogenase 7 family member A1	Often (30–79%)	In 1 condition
LONP1lon peptidase 1, mitochondrial	Often (30–79%)	In 1 condition
PDHA1pyruvate dehydrogenase E1 subunit alpha 1	Often (30–79%)	In 1 condition
PLPBPpyridoxal phosphate binding protein	Often (30–79%)	In 1 condition
PNPOpyridoxamine 5'-phosphate oxidase	Often (30–79%)	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

Abnormality of prenatal development or birth

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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