Adult central nervous system choriocarcinoma
diseaseOn this page
Also known as adult choriocarcinoma of the central nervous systemadult CNS choriocarcinomacentral nervous system choriocarcinomachoriocarcinoma of adult central nervous systemchoriocarcinoma of adult CNSchoriocarcinoma of the adult central nervous systemchoriocarcinoma of the adult CNSchoriocarcinoma of the central nervous system of adults
Summary
Adult central nervous system choriocarcinoma (MONDO:0003952) is a disease. A subtype of adult central nervous system germ cell tumor — 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 | adult central nervous system choriocarcinoma |
| Mondo ID | MONDO:0003952 |
| DOID | DOID:6634 |
| NCIT | C5793 |
| UMLS | C1370505 |
| MedGen | 234582 |
| GARD | 0023749 |
| Is cancer (heuristic) | no |
Also known as: adult central nervous system choriocarcinoma · adult choriocarcinoma of the central nervous system · adult CNS choriocarcinoma · central nervous system choriocarcinoma · choriocarcinoma of adult central nervous system · choriocarcinoma of adult CNS · choriocarcinoma of the adult central nervous system · choriocarcinoma of the adult CNS · choriocarcinoma of the central nervous system of adults
Disease family
This is a subtype of adult central nervous system germ cell tumor. 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 body system or component › nervous system disorder › central nervous system disorder › central nervous system neoplasm › central nervous system germ cell tumor › adult central nervous system germ cell tumor › adult central nervous system choriocarcinoma
Related subtypes (4): adult central nervous system teratoma, adult central nervous system embryonal carcinoma, adult central nervous system germinoma, adult central nervous system mixed germ cell 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.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.