Trait
Abnormal lymphocyte morphology
An abnormality of lymphocytes.
Summary
- Also called
- Abnormal lymphocytes, Abnormality of cells of the lymphoid lineage
Reference genomeGRCh38hg38
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Get my Genome Test15 genes linked to Abnormal lymphocyte morphology
Changes in these genes cause rare conditions in which Abnormal lymphocyte morphology 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 |
|---|---|---|
| ADAadenosine deaminase | Very often (80–99%) | In 1 condition |
| CD28CD28 molecule | Very often (80–99%) | In 2 conditions |
| CHD7chromodomain helicase DNA binding protein 7 | Very often (80–99%) | In 1 condition |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Very often (80–99%) | In 2 conditions |
| DCLRE1CDNA cross-link repair 1C | Very often (80–99%) | In 1 condition |
| IL2RGinterleukin 2 receptor subunit gamma | Very often (80–99%) | In 1 condition |
| IL7Rinterleukin 7 receptor | Very often (80–99%) | In 1 condition |
| NUDCD3NudC domain containing 3 | Very often (80–99%) | In 1 condition |
| PSMB10proteasome 20S subunit beta 10 | Very often (80–99%) | In 1 condition |
| RAG1recombination activating 1 | Very often (80–99%) | In 1 condition |
| RAG2recombination activating 2 | Very often (80–99%) | In 1 condition |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | Very often (80–99%) | In 1 condition |
| TNFRSF1BTNF receptor superfamily member 1B | Very often (80–99%) | In 2 conditions |
| NFKB2nuclear factor kappa B subunit 2 | Often (30–79%) | In 1 condition |
| TNFRSF13BTNF receptor superfamily member 13B | 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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