Trait
Recurring nosebleed
Clinical name: Spontaneous, recurrent epistaxis
Summary
- Also called
- Spontaneous, recurrent nosebleed, Recurrent epistaxes, Recurrent epistaxis
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page$trait$nameRead the genes linked to Recurring nosebleed, and the rest of your genome, with one test.
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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.
- Hereditary Hemorrhagic TelangiectasiaReads 4 of these genesACVRL1ENGGDF2SMAD4About this report →
- Inherited Platelet Function DisordersReads 5 of these genesITGA2BITGB3GP1BAGP1BBGP9About this report →
- ITGA2B/ITGB3-Related MacrothrombocytopeniaReads 2 of these genesITGA2BITGB3About this report →
- Chediak-Higashi syndromeReads 1 of these genesLYSTAbout this report →
Show 15 more reports
- Gaucher DiseaseReads 1 of these genesGBA1About this report →
- ITGB3-Related MacrothrombocytopeniaReads 1 of these genesITGB3About this report →
- Hereditary Von Willebrand DiseaseReads 1 of these genesGP1BAAbout this report →
- Juvenile Polyposis SyndromeReads 1 of these genesSMAD4About this report →
- Inherited ThrombocytopeniasReads 4 of these genesGNEGP1BBMYH9SRCAbout this report →
- Hermansky-Pudlak SyndromeReads 1 of these genesHPS3About this report →
- Lysosomal Storage DiseaseReads 2 of these genesGNEGBA1About this report →
- Parkinson DiseaseReads 1 of these genesGBA1About this report →
- Distal MyopathiesReads 1 of these genesGNEAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesMYH9About this report →
- Congenital Disorders of GlycosylationReads 1 of these genesGNEAbout this report →
- Other Inborn Errors of ImmunityReads 1 of these genesLYSTAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesLYSTAbout this report →
- Intellectual DisabilityReads 1 of these genesSMAD4About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesLYSTAbout this report →
Read the genes linked to Recurring nosebleed, and the rest of your genome, with one test.
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Get my Genome Test18 genes linked to Recurring nosebleed
Changes in these genes cause rare conditions in which Recurring nosebleed 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 |
|---|---|---|
| ACVRL1activin A receptor like type 1 | Always | In 2 conditions |
| DHRS3dehydrogenase/reductase 3 | Always | In 1 condition |
| ENGendoglin | Always | In 2 conditions |
| GDF2growth differentiation factor 2 | Always | In 2 conditions |
| GNEglucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | Always | In 1 condition |
| HPS3HPS3 biogenesis of lysosomal organelles complex 2 subunit 1 | Always | In 1 condition |
| ITGA2Bintegrin subunit alpha 2b | Very often (80–99%) | In 1 condition |
| ITGB3integrin subunit beta 3 | Very often (80–99%) | In 1 condition |
| SMAD4SMAD family member 4 | Very often (80–99%) | In 1 condition |
| GP1BAglycoprotein Ib platelet subunit alpha | Often (30–79%) | In 1 condition |
| GP1BBglycoprotein Ib platelet subunit beta | Often (30–79%) | In 1 condition |
| GP9glycoprotein IX platelet | Often (30–79%) | In 1 condition |
| MYH9myosin heavy chain 9 | Often (30–79%) | In 1 condition |
| PTPRJprotein tyrosine phosphatase receptor type J | Often (30–79%) | In 1 condition |
| TPM4tropomyosin 4 | Often (30–79%) | In 1 condition |
| GBA1glucosylceramidase beta 1 | Sometimes (5–29%) | In 1 condition |
| LYSTlysosomal trafficking regulator | Not recorded | In 1 condition |
| SRCSRC proto-oncogene, non-receptor tyrosine kinase | 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 2026.10.21-777c9289.
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