Trait
Anemic pallor
A type of pallor that is secondary to the presence of anemia.
Summary
- Also called
- Anaemic pallor
- Body system
- Abnormality of the integument
Reference genomeGRCh38hg38
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Get my Genome Test16 genes linked to Anemic pallor
Changes in these genes cause rare conditions in which Anemic pallor 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 |
|---|---|---|
| ALAS25'-aminolevulinate synthase 2 | Always | In 1 condition |
| BMPR1Abone morphogenetic protein receptor type 1A | Often (30–79%) | In 1 condition |
| ENGendoglin | Often (30–79%) | In 1 condition |
| SLC4A1solute carrier family 4 member 1 (Diego blood group) | Often (30–79%) | In 1 condition |
| SMAD4SMAD family member 4 | Often (30–79%) | In 1 condition |
| ALKALK receptor tyrosine kinase | Sometimes (5–29%) | In 1 condition |
| HACE1HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 | Sometimes (5–29%) | In 1 condition |
| LIN28Blin-28 RNA binding posttranscriptional regulator B | Sometimes (5–29%) | In 1 condition |
| LMO1LIM domain only 1 | Sometimes (5–29%) | In 1 condition |
| MYCNMYCN proto-oncogene, bHLH transcription factor | Sometimes (5–29%) | In 1 condition |
| PHOX2Bpaired like homeobox 2B | Sometimes (5–29%) | In 1 condition |
| TMPRSS6transmembrane serine protease 6 | Sometimes (5–29%) | In 1 condition |
| FANCAFA complementation group A | Not recorded | In 1 condition |
| FANCCFA complementation group C | Not recorded | In 1 condition |
| FANCD2FA complementation group D2 | Not recorded | In 1 condition |
| FANCEFA complementation group E | 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
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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