Parovarian cyst
disease diseaseOn this page
Also known as cyst, Paratubalcyst, parovariancysts, Paratubalcysts, parovarianhydatid cyst of Morgagnihydatid of MorgagniMorgagni hydatidMorgagni hydatid cystMorgagni hydatid cystsMorgagni HydatidsParatubal cystParatubal cystsparovarian cysts
Summary
Parovarian cyst (MONDO:0002965) is a disease. A subtype of embryonic cyst of fallopian tube — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | parovarian cyst |
| Mondo ID | MONDO:0002965 |
| MeSH | D010310 |
| DOID | DOID:4333 |
| SNOMED CT | 64233004 |
| UMLS | C0030584 |
| MedGen | 14622 |
| Is cancer (heuristic) | no |
Also known as: cyst, Paratubal · cyst, parovarian · cysts, Paratubal · cysts, parovarian · hydatid cyst of Morgagni · hydatid of Morgagni · Morgagni hydatid · Morgagni hydatid cyst · Morgagni hydatid cysts · Morgagni Hydatids · Paratubal cyst · Paratubal cysts · parovarian cysts
Disease family
Classification path: disease › human disease › disease by body system or component › reproductive system disorder › female reproductive system disorder › fallopian tube disorder › embryonic cyst of fallopian tube › parovarian cyst
Genetics & variants
GWAS landscape
No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.
Variant details and genetic-evidence tiers
No tiered GWAS variants or ClinVar records for this disease.
Genes & proteins
No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).
Function
No pathway enrichment — requires an associated-gene cohort.
Therapeutics
No druggable-target or therapeutic data for this disease’s cohort.
Clinical trials & evidence
Clinical trials
Clinical trials: 0.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.