Trait

Normochromic anemia

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

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39 genes linked to Normochromic anemia

Changes in these genes cause rare conditions in which Normochromic anemia 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
ABCD4ATP binding cassette subfamily D member 4	Always	In 1 condition
RPL15ribosomal protein L15	Always	In 2 conditions
SCARB2scavenger receptor class B member 2	Always	In 1 condition
UQCRFS1ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1	Always	In 1 condition
ASXL1ASXL transcriptional regulator 1	Often (30–79%)	In 1 condition
KITKIT proto-oncogene, receptor tyrosine kinase	Often (30–79%)	In 1 condition
SF3B1splicing factor 3b subunit 1	Often (30–79%)	In 1 condition
SRSF2serine and arginine rich splicing factor 2	Often (30–79%)	In 1 condition
TET2tet methylcytosine dioxygenase 2	Often (30–79%)	In 3 conditions
TREX1three prime repair exonuclease 1	Often (30–79%)	In 1 condition
ADA2adenosine deaminase 2	Sometimes (5–29%)	In 1 condition
GATA1GATA binding protein 1	Sometimes (5–29%)	In 1 condition
HEATR3HEAT repeat containing 3	Sometimes (5–29%)	In 1 condition
RPL11ribosomal protein L11	Sometimes (5–29%)	In 1 condition
RPL18ribosomal protein L18	Sometimes (5–29%)	In 1 condition
RPL26ribosomal protein L26	Sometimes (5–29%)	In 1 condition
RPL27ribosomal protein L27	Sometimes (5–29%)	In 1 condition
RPL31ribosomal protein L31	Sometimes (5–29%)	In 1 condition
RPL35ribosomal protein L35	Sometimes (5–29%)	In 1 condition
RPL35Aribosomal protein L35a	Sometimes (5–29%)	In 1 condition
RPL5ribosomal protein L5	Sometimes (5–29%)	In 1 condition
RPL8ribosomal protein L8	Sometimes (5–29%)	In 1 condition
RPL9ribosomal protein L9	Sometimes (5–29%)	In 1 condition
RPS10ribosomal protein S10	Sometimes (5–29%)	In 1 condition
RPS15Aribosomal protein S15a	Sometimes (5–29%)	In 1 condition
RPS17ribosomal protein S17	Sometimes (5–29%)	In 1 condition
RPS19ribosomal protein S19	Sometimes (5–29%)	In 1 condition
RPS20ribosomal protein S20	Sometimes (5–29%)	In 1 condition
RPS24ribosomal protein S24	Sometimes (5–29%)	In 1 condition
RPS26ribosomal protein S26	Sometimes (5–29%)	In 1 condition
RPS27ribosomal protein S27	Sometimes (5–29%)	In 1 condition
RPS28ribosomal protein S28	Sometimes (5–29%)	In 1 condition
RPS29ribosomal protein S29	Sometimes (5–29%)	In 1 condition
RPS7ribosomal protein S7	Sometimes (5–29%)	In 1 condition
TSR2TSR2 ribosome maturation factor	Sometimes (5–29%)	In 1 condition
ALDOAaldolase, fructose-bisphosphate A	Not recorded	In 1 condition
HK1hexokinase 1	Not recorded	In 1 condition
LCATlecithin-cholesterol acyltransferase	Not recorded	In 1 condition
TPI1triosephosphate isomerase 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.

Broader traits

Anemia of inadequate production

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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