Trait
Abnormally heavy bleeding during menstruation
Clinical name: Menorrhagia
Prolonged and excessive menses at regular intervals in excess of 80 mL or lasting longer than 7 days.
Summary
- Also called
- Abnormally heavy periods, Hypermenorrhea
This page as data
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page$trait$nameRead the genes linked to Abnormally heavy bleeding during menstruation, and the rest of your genome, with one test.
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Get my Genome Test43 genes linked to Abnormally heavy bleeding during menstruation
Changes in these genes cause rare conditions in which Abnormally heavy bleeding during menstruation 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 |
|---|---|---|
| APOLD1apolipoprotein L domain containing 1 | Always | In 1 condition |
| DTNBP1dystrobrevin binding protein 1 | Always | In 1 condition |
| F7coagulation factor VII | Always | In 2 conditions |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Always | In 1 condition |
| FYB1FYN binding protein 1 | Always | In 1 condition |
| GNEglucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | Always | In 1 condition |
| GP1BAglycoprotein Ib platelet subunit alpha | Always | In 3 conditions |
| HPS4HPS4 biogenesis of lysosomal organelles complex 3 subunit 2 | Always | In 1 condition |
| ITGB3integrin subunit beta 3 | Always | In 3 conditions |
| LRP6LDL receptor related protein 6 | Always | In 1 condition |
| PRKACGprotein kinase cAMP-activated catalytic subunit gamma | Always | In 1 condition |
| PTPRJprotein tyrosine phosphatase receptor type J | Always | In 1 condition |
| RASGRP2RAS guanyl releasing protein 2 | Always | In 1 condition |
| TPM4tropomyosin 4 | Very often (80–99%) | In 1 condition |
| BLOC1S3biogenesis of lysosomal organelles complex 1 subunit 3 | Often (30–79%) | In 1 condition |
| BLOC1S5biogenesis of lysosomal organelles complex 1 subunit 5 | Often (30–79%) | In 1 condition |
| F11coagulation factor XI | Often (30–79%) | In 1 condition |
| F8coagulation factor VIII | Often (30–79%) | In 2 conditions |
| GP1BBglycoprotein Ib platelet subunit beta | Often (30–79%) | In 2 conditions |
| GP9glycoprotein IX platelet | Often (30–79%) | In 2 conditions |
| HPS5HPS5 biogenesis of lysosomal organelles complex 2 subunit 2 | Often (30–79%) | In 1 condition |
| MYH9myosin heavy chain 9 | Often (30–79%) | In 2 conditions |
| PRLRprolactin receptor | Often (30–79%) | In 2 conditions |
| SERPINE1serpin family E member 1 | Often (30–79%) | In 2 conditions |
| ANO6anoctamin 6 | Sometimes (5–29%) | In 1 condition |
| DIAPH1diaphanous related formin 1 | Sometimes (5–29%) | In 1 condition |
| F10coagulation factor X | Sometimes (5–29%) | In 2 conditions |
| F13A1coagulation factor XIII A chain | Sometimes (5–29%) | In 1 condition |
| F13Bcoagulation factor XIII B chain | Sometimes (5–29%) | In 1 condition |
| F2coagulation factor II, thrombin | Sometimes (5–29%) | In 2 conditions |
| F5coagulation factor V | Sometimes (5–29%) | In 2 conditions |
| GGCXgamma-glutamyl carboxylase | Sometimes (5–29%) | In 1 condition |
| ITGA2Bintegrin subunit alpha 2b | Sometimes (5–29%) | In 2 conditions |
| LMAN1lectin, mannose binding 1 | Sometimes (5–29%) | In 1 condition |
| MCFD2multiple coagulation factor deficiency 2, ER cargo receptor complex subunit | Sometimes (5–29%) | In 2 conditions |
| SLC37A4solute carrier family 37 member 4 | Sometimes (5–29%) | In 1 condition |
| VKORC1vitamin K epoxide reductase complex subunit 1 | Sometimes (5–29%) | In 1 condition |
| PPP2R5Cprotein phosphatase 2 regulatory subunit B'gamma | Rarely (1–4%) | In 1 condition |
| GP6glycoprotein VI platelet | Not recorded | In 1 condition |
| NBEAL2neurobeachin like 2 | Not recorded | In 1 condition |
Show 3 more genes
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 2026.10.17-8666dff2.
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