Trait
Fetal polyuria
Abnormally increased production of urine by the fetus resulting in polyhydramnios.
Summary
- Also called
- Foetal polyuria
- Body system
- Abnormality of prenatal development or birth
Reference genomeGRCh38hg38
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Get my Genome Test12 genes linked to Fetal polyuria
Changes in these genes cause rare conditions in which Fetal polyuria 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 |
|---|---|---|
| FGF20fibroblast growth factor 20 | Often (30–79%) | In 1 condition |
| GFRA1GDNF family receptor alpha 1 | Often (30–79%) | In 1 condition |
| GREB1LGREB1 like retinoic acid receptor coactivator | Often (30–79%) | In 1 condition |
| ITGA8integrin subunit alpha 8 | Often (30–79%) | In 1 condition |
| RETret proto-oncogene | Often (30–79%) | In 1 condition |
| WNT9BWnt family member 9B | Often (30–79%) | In 1 condition |
| BSNDbarttin CLCNK type accessory subunit beta | Not recorded | In 1 condition |
| CLCNKAchloride voltage-gated channel Ka | Not recorded | In 1 condition |
| CLCNKBchloride voltage-gated channel Kb | Not recorded | In 1 condition |
| KCNJ1potassium inwardly rectifying channel subfamily J member 1 | Not recorded | In 1 condition |
| MAGED2MAGE family member D2 | 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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