Trait
Hyposthenuria
An abnormally low urinary specific gravity, i.e., reduced concentration of solutes in the urine.
Summary
- Also called
- Reduced urinary osmolality
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test10 genes linked to Hyposthenuria
Changes in these genes cause rare conditions in which Hyposthenuria 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 |
|---|---|---|
| ARNT2aryl hydrocarbon receptor nuclear translocator 2 | Always | In 1 condition |
| ATP6V1B1ATPase H+ transporting V1 subunit B1 | Always | In 1 condition |
| CLCN5Cl-/H+ antiporter 5 | Always | In 1 condition |
| CLDN16claudin 16 | Always | In 1 condition |
| AQP2aquaporin 2 | Very often (80–99%) | In 1 condition |
| AVPR2arginine vasopressin receptor 2 | Very often (80–99%) | In 2 conditions |
| UMODuromodulin | Often (30–79%) | In 1 condition |
| KCNJ1potassium inwardly rectifying channel subfamily J member 1 | Not recorded | In 1 condition |
| NPHP1nephrocystin 1 | Not recorded | In 1 condition |
| SLC12A1solute carrier family 12 member 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
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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