Trait

Neonatal sepsis

Systemic inflammatory response to infection in newborn babies.

Body system: Abnormality of the immune system

This page as data

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library(jsonlite)

url <- "https://dantelabs.com/traits/neonatal-sepsis.json"
page <- fromJSON(url)
page$trait$name

Open the JSON

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10 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.

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Every condition report

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7 genes linked to Neonatal sepsis

Changes in these genes cause rare conditions in which Neonatal sepsis 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
AK2adenylate kinase 2	Always	In 1 condition
G6PC3glucose-6-phosphatase catalytic subunit 3	Often (30–79%)	In 1 condition
COG4component of oligomeric golgi complex 4	Sometimes (5–29%)	In 1 condition
IL7Rinterleukin 7 receptor	Sometimes (5–29%)	In 1 condition
ALDH3A2aldehyde dehydrogenase 3 family member A2	Rarely (1–4%)	In 1 condition
SPINK5serine peptidase inhibitor Kazal type 5	Rarely (1–4%)	In 1 condition
SERAC1serine active site containing 1	Not recorded	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.

Broader traits

Infection in blood stream

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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