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Trait
Small amount of blood in urine
Clinical name: Microscopic hematuria
Microscopic hematuria detected by dipstick or microscopic examination of the urine.
Summary
- Also called
- Microhematuria, Occult hematuria
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This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/microscopic-hematuria.json"
page <- fromJSON(url)
page$trait$nameSmall amount of blood in urineHP:0002907
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Get my Genome Test43 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Alport SyndromeReads 3 of these genesCOL4A3COL4A5COL4A4About this report →
- Hereditary Wilms TumourReads 2 of these genesRESTWT1About this report →
- Congenital Thrombotic Thrombocytopenic PurpuraReads 1 of these genesADAMTS13About this report →
- CystinosisReads 1 of these genesCTNSAbout this report →
Show 39 more reports
- Nail-Patella SyndromeReads 1 of these genesLMX1BAbout this report →
- PBX1-Related Kidney and Urinary Tract AnomaliesReads 1 of these genesPBX1About this report →
- Perlman SyndromeReads 1 of these genesDIS3L2About this report →
- Simpson-Golabi-Behmel SyndromeReads 1 of these genesGPC3About this report →
- GlomerulosclerosisReads 2 of these genesPAX2INF2About this report →
- Dent Disease and Lowe SyndromeReads 1 of these genesCLCN5About this report →
- Hereditary Breast and Ovarian Cancer (BRCA1/2)Reads 1 of these genesBRCA2About this report →
- Hereditary Gingival FibromatosisReads 1 of these genesRESTAbout this report →
- Focal Segmental GlomerulosclerosisReads 2 of these genesPAX2INF2About this report →
- Immuno-Osseous DysplasiasReads 1 of these genesSMARCAL1About this report →
- Mosaic Variegated Aneuploidy SyndromeReads 1 of these genesTRIP13About this report →
- Hereditary HypolipoproteinemiasReads 1 of these genesAPOA1About this report →
- Nephrotic SyndromeReads 2 of these genesNOS1APNUP85About this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 1 of these genesFN1About this report →
- Hemolytic Uremic Syndrome, Interstitial NephritisReads 1 of these genesCFHR5About this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 1 of these genesH19About this report →
- Kidney CancerReads 1 of these genesTRIM28About this report →
- ThrombophiliaReads 1 of these genesF2About this report →
- Rare Inherited Coagulation Factor DeficienciesReads 1 of these genesF2About this report →
- Congenital Anomalies of the Kidney and Urinary TractReads 1 of these genesPAX2About this report →
- Familial HypomagnesemiaReads 1 of these genesCLDN16About this report →
- Hereditary AmyloidosisReads 1 of these genesAPOA1About this report →
- Urinary and Renal System TumourReads 1 of these genesTRIM28About this report →
- Glycogen Storage DiseaseReads 1 of these genesSLC37A4About this report →
- Fanconi AnemiaReads 1 of these genesBRCA2About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesWT1About this report →
- Homocystinuria & Cobalamin DisordersReads 1 of these genesCUBNAbout this report →
- Inherited ThrombocytopeniasReads 1 of these genesADAMTS13About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesLPIN2About this report →
- DNA Repair DiseaseReads 1 of these genesBRCA2About this report →
- Female InfertilityReads 1 of these genesTRIP13About this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesAPOA1INF2About this report →
- Lysosomal Storage DiseaseReads 1 of these genesCTNSAbout this report →
- Hypertrophic CardiomyopathyReads 1 of these genesH19About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesINF2About this report →
- Congenital Disorders of GlycosylationReads 1 of these genesSLC37A4About this report →
- Epilepsy (Full Panel)Reads 1 of these genesLMNB2About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesSMARCAL1About this report →
- Intellectual DisabilityReads 1 of these genesACSL4About this report →
Read the genes linked to Small amount of blood in urine, and the rest of your genome, with one test.
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Get my Genome Test37 genes linked to Small amount of blood in urine
Changes in these genes cause rare conditions in which Small amount of blood in urine 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 |
|---|---|---|
| APOA1apolipoprotein A1 | Always | In 1 condition |
| CFHR5complement factor H related 5 | Always | In 1 condition |
| COL4A3collagen type IV alpha 3 chain | Always | In 4 conditions |
| CUBNcubilin | Always | In 1 condition |
| NOS1APnitric oxide synthase 1 adaptor protein | Always | In 1 condition |
| NUP85nucleoporin 85 | Always | In 1 condition |
| OAS22'-5'-oligoadenylate synthetase 2 | Always | In 1 condition |
| SLC37A4solute carrier family 37 member 4 | Always | In 1 condition |
| ACSL4acyl-CoA synthetase long chain family member 4 | Very often (80–99%) | In 1 condition |
| AMMECR1AMMECR nuclear protein 1 | Very often (80–99%) | In 1 condition |
| COL4A5collagen type IV alpha 5 chain | Very often (80–99%) | In 2 conditions |
| FN1fibronectin 1 | Very often (80–99%) | In 2 conditions |
| KCNE5potassium voltage-gated channel subfamily E regulatory subunit 5 | Very often (80–99%) | In 1 condition |
| LMX1BLIM homeobox transcription factor 1 beta | Very often (80–99%) | In 1 condition |
| BRCA2BRCA2 DNA repair associated | Sometimes (5–29%) | In 1 condition |
| CLDN16claudin 16 | Sometimes (5–29%) | In 1 condition |
| CTNScystinosin, lysosomal cystine transporter | Sometimes (5–29%) | In 2 conditions |
| CTR9CTR9 component of Paf1/RNA polymerase II complex | Sometimes (5–29%) | In 1 condition |
| DIS3L2DIS3 like 3'-5' exoribonuclease 2 | Sometimes (5–29%) | In 1 condition |
| F2coagulation factor II, thrombin | Sometimes (5–29%) | In 1 condition |
| GPC3glypican 3 | Sometimes (5–29%) | In 1 condition |
| H19H19 imprinted maternally expressed transcript | Sometimes (5–29%) | In 1 condition |
| LMNB2lamin B2 | Sometimes (5–29%) | In 1 condition |
| LPIN2lipin 2 | Sometimes (5–29%) | In 1 condition |
| PAX2paired box 2 | Sometimes (5–29%) | In 1 condition |
| PBX1PBX homeobox 1 | Sometimes (5–29%) | In 1 condition |
| POU6F2POU class 6 homeobox 2 | Sometimes (5–29%) | In 1 condition |
| RESTRE1 silencing transcription factor | Sometimes (5–29%) | In 1 condition |
| SMARCAL1SNF2 related chromatin remodeling annealing helicase 1 | Sometimes (5–29%) | In 1 condition |
| TRIM28tripartite motif containing 28 | Sometimes (5–29%) | In 1 condition |
| TRIP13thyroid hormone receptor interactor 13 | Sometimes (5–29%) | In 1 condition |
| WT1WT1 transcription factor | Sometimes (5–29%) | In 1 condition |
| ADAMTS13ADAM metallopeptidase with thrombospondin type 1 motif 13 | Not recorded | In 1 condition |
| CLCN5Cl-/H+ antiporter 5 | Not recorded | In 3 conditions |
| COL4A4collagen type IV alpha 4 chain | Not recorded | In 1 condition |
| INF2inverted formin 2 | Not recorded | In 1 condition |
| PRODH2proline dehydrogenase 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 2026.10.19-9814e911.
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