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Trait
Ovarian cyst
The presence of one or more cysts of the ovary.
Summary
- Also called
- Cystic abnormalities of the ovaries, Cystic ovaries, Ovarian cystic abnormality
- Body system
- Abnormality of the genitourinary system
Ovarian cystHP:0000138
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Read the genes linked to Ovarian cyst, and the rest of your genome, with one test.
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Get my Genome Test19 genes linked to Ovarian cyst
Changes in these genes cause rare conditions in which Ovarian cyst 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 |
|---|---|---|
| INSRinsulin receptor | Always | In 1 condition |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Always | In 1 condition |
| GNASGNAS complex locus | Very often (80–99%) | In 1 condition |
| CYP17A1cytochrome P450 family 17 subfamily A member 1 | Often (30–79%) | In 1 condition |
| FSHRfollicle stimulating hormone receptor | Often (30–79%) | In 1 condition |
| PDE11Aphosphodiesterase 11A | Often (30–79%) | In 2 conditions |
| PORcytochrome p450 oxidoreductase | Often (30–79%) | In 1 condition |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Often (30–79%) | In 1 condition |
| F7coagulation factor VII | Sometimes (5–29%) | In 1 condition |
| MSH3mutS homolog 3 | Sometimes (5–29%) | In 1 condition |
| NTHL1nth like DNA glycosylase 1 | Sometimes (5–29%) | In 1 condition |
| TBX1T-box transcription factor 1 | Sometimes (5–29%) | In 1 condition |
| TRPV6transient receptor potential cation channel subfamily V member 6 | Sometimes (5–29%) | In 1 condition |
| CYP19A1cytochrome P450 family 19 subfamily A member 1 | Not recorded | In 1 condition |
| LHBluteinizing hormone subunit beta | Not recorded | In 1 condition |
| OFD1OFD1 centriole and centriolar satellite protein | Not recorded | In 1 condition |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Not recorded | In 1 condition |
| PTENphosphatase and tensin homolog | Not recorded | In 1 condition |
| STK11serine/threonine kinase 11 | 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.
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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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