Trait
Multinodular goiter
Enlargement of the thyroid gland related to multiple nodules in the thyroid gland.
Summary
- Also called
- Multinodular goitre
- Body system
- Abnormality of the endocrine system
Reference genomeGRCh38hg38
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Get my Genome Test9 genes linked to Multinodular goiter
Changes in these genes cause rare conditions in which Multinodular goiter 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 |
|---|---|---|
| DICER1dicer 1, ribonuclease III | Always | In 2 conditions |
| KEAP1kelch like ECH associated protein 1 | Always | In 1 condition |
| MAD1L1mitotic arrest deficient 1 like 1 | Always | In 1 condition |
| TGthyroglobulin | Always | In 1 condition |
| AIPAHR interacting HSP90 co-chaperone | Often (30–79%) | In 1 condition |
| GPR101G protein-coupled receptor 101 | Often (30–79%) | In 1 condition |
| SASH1SAM and SH3 domain containing 1 | Often (30–79%) | In 1 condition |
| ALMS1ALMS1 centrosome and basal body associated protein | Not recorded | In 1 condition |
| NKX2-1NK2 homeobox 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
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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