Trait
Hashimoto thyroiditis
A chronic, autoimmune type of thyroiditis associated with hypothyroidism.
Summary
- Also called
- Chronic lymphocytic thyroiditis, Hashimoto's thyroiditis
Reference genomeGRCh38hg38
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Get my Genome Test20 genes linked to Hashimoto thyroiditis
Changes in these genes cause rare conditions in which Hashimoto thyroiditis 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 |
|---|---|---|
| CDKN1Bcyclin dependent kinase inhibitor 1B | Always | In 1 condition |
| FEM1Bfem-1 homolog B | Always | In 1 condition |
| IL18BPinterleukin 18 binding protein | Always | In 1 condition |
| ITCHitchy E3 ubiquitin protein ligase | Always | In 1 condition |
| FOXD3forkhead box D3 | Often (30–79%) | In 1 condition |
| POLGDNA polymerase gamma, catalytic subunit | Often (30–79%) | In 1 condition |
| STAT5Bsignal transducer and activator of transcription 5B | Often (30–79%) | In 1 condition |
| ADA2adenosine deaminase 2 | Sometimes (5–29%) | In 1 condition |
| AIREautoimmune regulator | Sometimes (5–29%) | In 1 condition |
| PLCG2phospholipase C gamma 2 | Sometimes (5–29%) | In 1 condition |
| PTENphosphatase and tensin homolog | Sometimes (5–29%) | In 1 condition |
| TBX2T-box transcription factor 2 | Sometimes (5–29%) | In 1 condition |
| CLCNKBchloride voltage-gated channel Kb | Rarely (1–4%) | In 1 condition |
| DCLRE1CDNA cross-link repair 1C | Rarely (1–4%) | In 1 condition |
| MYT1Lmyelin transcription factor 1 like | Rarely (1–4%) | In 1 condition |
| PI4KAphosphatidylinositol 4-kinase alpha | Rarely (1–4%) | In 1 condition |
| SLC12A3solute carrier family 12 member 3 | Rarely (1–4%) | In 1 condition |
| TTC7Atetratricopeptide repeat domain 7A | Rarely (1–4%) | In 1 condition |
| C1Scomplement C1s | Not recorded | In 1 condition |
| SEC23BSEC23 homolog B, COPII component | 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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