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Traits
Traits linked to UMOD
uromodulin
The Human Phenotype Ontology links 31 traits to UMOD, by body system: features seen in people with one of the gene's rare conditions.
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Abnormality of the genitourinary system
| Trait | How often it is seen |
|---|---|
| Chronic kidney disease | Always |
| Renal failure | Always |
| Renal tubular atrophy | Always |
| Stage 2 chronic kidney disease | Always |
| Stage 3 chronic kidney disease | Always |
| Stage 4 chronic kidney disease | Always |
| Tubulointerstitial nephritis | Always |
| Decreased glomerular filtration rate | Very often (80–99%) |
| Renal interstitial fibrosis | Very often (80–99%) |
| Cystic kidney disease | Often (30–79%) |
| Glomerular sclerosis | Often (30–79%) |
| Increased urine output | Often (30–79%) |
| Renal corticomedullary cysts | Often (30–79%) |
| Small kidneys | Often (30–79%) |
| Stage 1 chronic kidney disease | Often (30–79%) |
| Stage 5 chronic kidney disease | Often (30–79%) |
| Thickened glomerular basement membrane | Often (30–79%) |
| Hyperechogenic kidneys | Sometimes (5–29%) |
| Reduced renal corticomedullary differentiation | Sometimes (5–29%) |
| Kidney inflammation | Not recorded |
Laboratory abnormality
| Trait | How often it is seen |
|---|---|
| Decreased urinary urate | Always |
| Elevated circulating parathyroid hormone level | Always |
| Increased blood urea nitrogen | Always |
| Metabolic acidosis | Always |
| Elevated creatinine | Very often (80–99%) |
| High blood uric acid level | Often (30–79%) |
| High urine protein levels | Often (30–79%) |
| Hyposthenuria | Often (30–79%) |
| Blood in urine | Sometimes (5–29%) |
Abnormality of the cardiovascular system
| Trait | How often it is seen |
|---|---|
| High blood pressure | Often (30–79%) |
Abnormality of the musculoskeletal system
| Trait | How often it is seen |
|---|---|
| Gout | Often (30–79%) |
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.
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to UMOD and how often each is seen. Find out more at hpo.jax.org.
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