Trait
Hydatidiform mole
Hydatidiform mole (HM) is an aberrant human pregnancy with absence of, or abnormal embryonic development, hydropic degeneration of chorionic villi, and excessive proliferation of the trophoblast.
Summary
- Body system
- Abnormality of prenatal development or birth
Reference genomeGRCh38hg38
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Get my Genome Test4 genes linked to Hydatidiform mole
Changes in these genes cause rare conditions in which Hydatidiform mole 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 |
|---|---|---|
| KHDC3LKH domain containing 3 like, subcortical maternal complex member | Always | In 1 condition |
| MEI1meiotic double-stranded break formation protein 1 | Always | In 1 condition |
| NLRP7NLR family pyrin domain containing 7 | Always | In 1 condition |
| TOP6BLTOP6B like initiator of meiotic double strand breaks | Always | 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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