Trait

Erythroid hypoplasia

Decreased count of erythroid precursor cells, that is, erythroid lineage cells in the bone marrow.

Also called: Erythroblastopenia
Body system: Abnormality of blood and blood-forming tissues

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11 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.

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31 genes linked to Erythroid hypoplasia

Changes in these genes cause rare conditions in which Erythroid hypoplasia 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
HEATR3HEAT repeat containing 3	Always	In 2 conditions
RPL18ribosomal protein L18	Always	In 2 conditions
TCN2transcobalamin 2	Always	In 1 condition
TP53tumor protein p53	Always	In 1 condition
ADA2adenosine deaminase 2	Often (30–79%)	In 1 condition
GATA1GATA binding protein 1	Often (30–79%)	In 1 condition
RPL11ribosomal protein L11	Often (30–79%)	In 1 condition
RPL15ribosomal protein L15	Often (30–79%)	In 1 condition
RPL26ribosomal protein L26	Often (30–79%)	In 1 condition
RPL27ribosomal protein L27	Often (30–79%)	In 1 condition
RPL31ribosomal protein L31	Often (30–79%)	In 1 condition
RPL35ribosomal protein L35	Often (30–79%)	In 1 condition
RPL35Aribosomal protein L35a	Often (30–79%)	In 2 conditions
RPL5ribosomal protein L5	Often (30–79%)	In 1 condition
RPL8ribosomal protein L8	Often (30–79%)	In 1 condition
RPL9ribosomal protein L9	Often (30–79%)	In 1 condition
RPS10ribosomal protein S10	Often (30–79%)	In 1 condition
RPS14ribosomal protein S14	Often (30–79%)	In 2 conditions
RPS15Aribosomal protein S15a	Often (30–79%)	In 2 conditions
RPS17ribosomal protein S17	Often (30–79%)	In 2 conditions
RPS19ribosomal protein S19	Often (30–79%)	In 1 condition
RPS20ribosomal protein S20	Often (30–79%)	In 1 condition
RPS24ribosomal protein S24	Often (30–79%)	In 1 condition
RPS26ribosomal protein S26	Often (30–79%)	In 1 condition
RPS27ribosomal protein S27	Often (30–79%)	In 1 condition
RPS28ribosomal protein S28	Often (30–79%)	In 1 condition
RPS29ribosomal protein S29	Often (30–79%)	In 1 condition
RPS7ribosomal protein S7	Often (30–79%)	In 1 condition
TET2tet methylcytosine dioxygenase 2	Often (30–79%)	In 1 condition
TSR2TSR2 ribosome maturation factor	Often (30–79%)	In 1 condition
G6PC3glucose-6-phosphatase catalytic subunit 3	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

Abnormal number of erythroid precursors

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 2026.10.21-311f020e.

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