Skip to content
Use your HSA or FSA funds

Trait

Abnormal fallopian tube morphology

An abnormality of the fallopian tube.

HPO HP:0011027

Summary

Also called
Abnormality of the fallopian tube
Body system
Abnormality of the genitourinary system

23 genes linked to Abnormal fallopian tube morphology

Changes in these genes cause rare conditions in which Abnormal fallopian tube morphology 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.

GeneHow often it is seenConditions
ATMATM serine/threonine kinaseVery often (80–99%)In 1 condition
BARD1BRCA1 associated RING domain 1Very often (80–99%)In 1 condition
BRCA1BRCA1 DNA repair associatedVery often (80–99%)In 1 condition
BRCA2BRCA2 DNA repair associatedVery often (80–99%)In 1 condition
BRIP1BRCA1 interacting DNA helicase 1Very often (80–99%)In 1 condition
CHEK2checkpoint kinase 2Very often (80–99%)In 1 condition
MRE11MRE11 double strand break repair nucleaseVery often (80–99%)In 1 condition
NBNnibrinVery often (80–99%)In 1 condition
PALB2partner and localizer of BRCA2Very often (80–99%)In 1 condition
PTENphosphatase and tensin homologVery often (80–99%)In 1 condition
RAD50RAD50 double strand break repair proteinVery often (80–99%)In 1 condition
RAD51RAD51 recombinaseVery often (80–99%)In 1 condition
RAD51CRAD51 paralog CVery often (80–99%)In 1 condition
RAD51DRAD51 paralog DVery often (80–99%)In 1 condition
TP53tumor protein p53Very often (80–99%)In 1 condition
WT1WT1 transcription factorVery often (80–99%)In 1 condition
COX7Bcytochrome c oxidase subunit 7BSometimes (5–29%)In 1 condition
FANCBFA complementation group BSometimes (5–29%)In 1 condition
HCCSholocytochrome c synthaseSometimes (5–29%)In 1 condition
HYLS1HYLS1 centriolar and ciliogenesis associatedSometimes (5–29%)In 1 condition
KIF7kinesin family member 7Sometimes (5–29%)In 1 condition
NDUFB11NADH:ubiquinone oxidoreductase subunit B11Sometimes (5–29%)In 1 condition
PLGplasminogenSometimes (5–29%)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.

Narrower traits

Broader traits

Abnormal morphology of female internal genitalia

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.

One test. A lifetime of answers.

From $449Free shipping · Results in 6–8 weeks

Get my Genome Test