Trait

Paralytic ileus

HPO HP:0002590

Body system: Abnormality of the digestive system

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4 genes linked to Paralytic ileus

Changes in these genes cause rare conditions in which Paralytic ileus 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
ARPC5actin related protein 2/3 complex subunit 5	Often (30–79%)	In 1 condition
MTRFRmitochondrial translation release factor in rescue	Often (30–79%)	In 2 conditions
FAHfumarylacetoacetate hydrolase	Not recorded	In 1 condition
HMBShydroxymethylbilane synthase	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

Ileus

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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