Trait
Erythroid hyperplasia
Increased count of erythroid precursor cells, that is, erythroid lineage cells in the bone marrow.
Summary
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Erythroid hyperplasia, and the rest of your genome, with one test.
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Get my Genome Test20 genes linked to Erythroid hyperplasia
Changes in these genes cause rare conditions in which Erythroid hyperplasia 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 |
|---|---|---|
| ABCB7ATP binding cassette subfamily B member 7 | Always | In 1 condition |
| CDAN1codanin 1 | Always | In 1 condition |
| GATA1GATA binding protein 1 | Always | In 2 conditions |
| KLF1KLF transcription factor 1 | Always | In 2 conditions |
| LARS2leucyl-tRNA synthetase 2, mitochondrial | Always | In 1 condition |
| LPIN2lipin 2 | Always | In 1 condition |
| NHEJ1non-homologous end joining factor 1 | Always | In 1 condition |
| PGK1phosphoglycerate kinase 1 | Always | In 1 condition |
| PKLRpyruvate kinase L/R | Always | In 1 condition |
| SLC11A2solute carrier family 11 member 2 | Always | In 1 condition |
| HBBhemoglobin subunit beta | Often (30–79%) | In 1 condition |
| SF3B1splicing factor 3b subunit 1 | Often (30–79%) | In 1 condition |
| TET2tet methylcytosine dioxygenase 2 | Often (30–79%) | In 1 condition |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Sometimes (5–29%) | In 1 condition |
| URODuroporphyrinogen decarboxylase | Sometimes (5–29%) | In 1 condition |
| UROSuroporphyrinogen III synthase | Sometimes (5–29%) | In 1 condition |
| CDIN1CDAN1 interacting nuclease 1 | Not recorded | In 1 condition |
| ERBB3erb-b2 receptor tyrosine kinase 3 | Not recorded | In 1 condition |
| GLRX5glutaredoxin 5 | Not recorded | In 1 condition |
| PUS1pseudouridine synthase 1 | 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.
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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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