Trait
Secondary hyperparathyroidism
Secondary hyperparathyroidism refers to the production of higher than normal levels of parathyroid hormone in the presence of hypocalcemia.
Summary
- Body system
- Abnormality of the endocrine system
Reference genomeGRCh38hg38
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Get my Genome Test5 genes linked to Secondary hyperparathyroidism
Changes in these genes cause rare conditions in which Secondary hyperparathyroidism 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 |
|---|---|---|
| CYP27B1cytochrome P450 family 27 subfamily B member 1 | Very often (80–99%) | In 2 conditions |
| CYP2R1cytochrome P450 family 2 subfamily R member 1 | Very often (80–99%) | In 1 condition |
| CA2carbonic anhydrase 2 | Sometimes (5–29%) | In 1 condition |
| PHEXphosphate regulating endopeptidase X-linked | Sometimes (5–29%) | In 1 condition |
| VDRvitamin D receptor | 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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