Trait
Low blood uric acid levels
Clinical name: Hypouricemia
The concentration of uric acid in the blood circulation is below the lower limit of normal.
Summary
- Also called
- Decreased uric acid concentration, Decreased uric acid level, Decreased uric acid level in blood, Reduced uric acid concentration, Reduced uric acid level, Reduced uric acid level in blood
- Body system
- Laboratory abnormality
Reference genomeGRCh38hg38
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Get my Genome Test17 genes linked to Low blood uric acid levels
Changes in these genes cause rare conditions in which Low blood uric acid levels 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 |
|---|---|---|
| ATP7BATPase copper transporting beta | Always | In 1 condition |
| GPHNgephyrin | Always | In 1 condition |
| MOCOSmolybdenum cofactor sulfurase | Always | In 1 condition |
| MOCS2molybdenum cofactor synthesis 2 | Always | In 1 condition |
| PNPpurine nucleoside phosphorylase | Always | In 2 conditions |
| SLC22A12solute carrier family 22 member 12 | Always | In 2 conditions |
| SLC2A9solute carrier family 2 member 9 | Always | In 2 conditions |
| XDHxanthine dehydrogenase | Always | In 1 condition |
| EHHADHenoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase | Often (30–79%) | In 1 condition |
| GATMglycine amidinotransferase | Often (30–79%) | In 1 condition |
| NDUFAF6NADH:ubiquinone oxidoreductase complex assembly factor 6 | Often (30–79%) | In 1 condition |
| PRPS1phosphoribosyl pyrophosphate synthetase 1 | Often (30–79%) | In 1 condition |
| SLC34A1solute carrier family 34 member 1 | Often (30–79%) | In 1 condition |
| CTNScystinosin, lysosomal cystine transporter | Sometimes (5–29%) | In 1 condition |
| HNF4Ahepatocyte nuclear factor 4 alpha | Not recorded | In 1 condition |
| MOCS1molybdenum cofactor synthesis 1 | Not recorded | In 1 condition |
| SLC2A2solute carrier family 2 member 2 | 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
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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