Trait
Hepatic calcification
The presence of abnormal calcium deposition in the liver.
Summary
- Also called
- Liver calcifications
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test6 genes linked to Hepatic calcification
Changes in these genes cause rare conditions in which Hepatic calcification 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 |
|---|---|---|
| LYNLYN proto-oncogene, Src family tyrosine kinase | Always | In 1 condition |
| ABCC6ATP binding cassette subfamily C member 6 | Very often (80–99%) | In 1 condition |
| ENPP1ectonucleotide pyrophosphatase/phosphodiesterase 1 | Very often (80–99%) | In 1 condition |
| CPT2carnitine palmitoyltransferase 2 | Often (30–79%) | In 2 conditions |
| RRAGDRas related GTP binding D | Often (30–79%) | In 1 condition |
| LBRlamin B 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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