Low-grade neuroendocrine tumor of the corpus uteri

disease
On this page

Also known as low-grade neuroendocrine tumor of the uterine corpuslow-grade neuroendocrine tumour of the uterine corpuswell-differentiated neuroendocrine neoplasm of the endometriumwell-differentiated neuroendocrine tumor of the corpus uteriwell-differentiated neuroendocrine tumor of the endometriumwell-differentiated neuroendocrine tumour of the corpus uteriwell-differentiated neuroendocrine tumour of the endometrium

Summary

Low-grade neuroendocrine tumor of the corpus uteri (MONDO:0016270) is a cancer. A subtype of uterine corpus cancer — 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

FieldValue
Canonical namelow-grade neuroendocrine tumor of the corpus uteri
Mondo IDMONDO:0016270
Orphanet213736
NCITC126773
UMLSC5190779
MedGen1672976
GARD0020483
Is cancer (heuristic)yes

Also known as: low-grade neuroendocrine tumor of the uterine corpus · low-grade neuroendocrine tumour of the uterine corpus · well-differentiated neuroendocrine neoplasm of the endometrium · well-differentiated neuroendocrine tumor of the corpus uteri · well-differentiated neuroendocrine tumor of the endometrium · well-differentiated neuroendocrine tumour of the corpus uteri · well-differentiated neuroendocrine tumour of the endometrium

Disease family

This is a subtype of uterine corpus cancer. 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: human disease › disease by etiologic mechanism › cancer or benign tumorneoplastic disease or syndromeneoplasmcancerreproductive system cancerfemale reproductive organ canceruterine canceruterine corpus cancerlow-grade neuroendocrine tumor of the corpus uteri

Related subtypes (11): uterine corpus endometrial carcinoma, uterine body mixed cancer, uterine corpus sarcoma, endometrial serous adenocarcinoma, squamous cell carcinoma of the corpus uteri, undifferentiated carcinoma of the corpus uteri, papillary carcinoma of the corpus uteri, high-grade neuroendocrine carcinoma of the corpus uteri, adenoid cystic carcinoma of the corpus uteri, transitional cell carcinoma of the corpus uteri, malignant germ cell tumor of corpus uteri

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.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.