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Trait

Macular hemorrhage

Bleeding occurring within the macula lutea of the retina.

HPO HP:0025574

Summary

Also called
Macular haemorrhage
Body system
Abnormality of blood and blood-forming tissuesAbnormality of the cardiovascular systemAbnormality of the eye

7 genes linked to Macular hemorrhage

Changes in these genes cause rare conditions in which Macular hemorrhage 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.

GeneHow often it is seenConditions
APOEapolipoprotein ESometimes (5–29%)In 1 condition
CFHcomplement factor HSometimes (5–29%)In 1 condition
CFHR1complement factor H related 1Sometimes (5–29%)In 1 condition
CFHR3complement factor H related 3Sometimes (5–29%)In 1 condition
CFIcomplement factor ISometimes (5–29%)In 1 condition
EFEMP1EGF-like fibulin extracellular matrix protein 1Sometimes (5–29%)In 1 condition
HMCN1hemicentin 1Sometimes (5–29%)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

Abnormal macular morphologyRetinal bleeding

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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