Non-gestational choriocarcinoma

Summary

Non-gestational choriocarcinoma (MONDO:0006871) is a disease. A subtype of choriocarcinoma — 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	non-gestational choriocarcinoma
Mondo ID	MONDO:0006871
EFO	EFO:1001064
MeSH	D031954
DOID	DOID:4320
UMLS	C1135873
MedGen	211656
GARD	0024494
Is cancer (heuristic)	no

Disease family

This is a subtype of choriocarcinoma. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by etiologic mechanism › cancer or benign tumor › neoplastic disease or syndrome › neoplasm › trophoblastic neoplasm › choriocarcinoma › non-gestational choriocarcinoma

Related subtypes (7): pulmonary artery choriocarcinoma, choriocarcinoma of ovary, choriocarcinoma of testis, gastric choriocarcinoma, choriocarcinoma of the central nervous system, gestational choriocarcinoma, placental site trophoblastic tumor

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.