Trait

Hypoamylasemia

The concentration of amylase in the blood circulation is below the lower limit of normal.

Also called: Decreased circulating amylase level
Body system: Laboratory abnormality

This page as data

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library(jsonlite)

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

Open the JSON

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4 genes linked to Hypoamylasemia

Changes in these genes cause rare conditions in which Hypoamylasemia 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
CNOT1CCR4-NOT transcription complex subunit 1	Often (30–79%)	In 1 condition
DNAJC21DnaJ heat shock protein family (Hsp40) member C21	Often (30–79%)	In 1 condition
EFL1elongation factor like GTPase 1	Often (30–79%)	In 1 condition
SBDSSBDS ribosome maturation factor	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.

Broader traits

Abnormal circulating amylase concentration

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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