Trait
Compensated hypothyroidism
Condition associated with a raised serum concentration of thyroid stimulating hormone (TSH) but a normal serum free thyroxine (FT4).
Summary
- Also called
- Mild hypothyroidism, Subclinical hypothyroidism
- Body system
- Abnormality of the endocrine system
Reference genomeGRCh38hg38
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Get my Genome Test9 genes linked to Compensated hypothyroidism
Changes in these genes cause rare conditions in which Compensated hypothyroidism 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 |
|---|---|---|
| THRBthyroid hormone receptor beta | Always | In 1 condition |
| TANGO2transport and golgi organization 2 homolog | Often (30–79%) | In 1 condition |
| TREX1three prime repair exonuclease 1 | Often (30–79%) | In 1 condition |
| NKX2-1NK2 homeobox 1 | Sometimes (5–29%) | In 2 conditions |
| TSHRthyroid stimulating hormone receptor | Sometimes (5–29%) | In 1 condition |
| FOXI1forkhead box I1 | Not recorded | In 1 condition |
| KCNJ10potassium inwardly rectifying channel subfamily J member 10 | Not recorded | In 1 condition |
| SLC26A4solute carrier family 26 member 4 | Not recorded | In 1 condition |
| TGthyroglobulin | 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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