Placenta neoplasm

Summary

Placenta neoplasm (MONDO:0021218) is a cancer. A subtype of placenta disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

• Classification: Cancer

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	placenta neoplasm
Mondo ID	MONDO:0021218
NCIT	C4858
UMLS	C0524541
MedGen	105551
Anatomy (UBERON)	UBERON:0001987
Is cancer (heuristic)	yes

Also known as: neoplasm of placenta · neoplasm of the placenta · placenta neoplasm (disease) · placenta neoplasms · placenta tumor · placenta tumors · placenta tumour · placenta tumours · placental neoplasm · placental tumor · placental tumors · placental tumour · placental tumours · trophoblastic tumor placental site · trophoblastic tumour placental site · tumor of placenta · tumor of the placenta · tumour of placenta · tumour of the placenta

Disease family

This is a subtype of placenta disorder. 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 › reproductive system disorder › female reproductive system disorder › uterine disorder › placenta disorder › placenta neoplasm

Related subtypes (7): placental abruption, fetal growth restriction, oligohydramnios, placenta accreta, placenta praevia, placental insufficiency, disorder of extraembryonic membrane

Subtypes (3): placenta cancer, hydatidiform mole, benign neoplasm of placenta

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.