Squamous cell carcinoma of the corpus uteri

disease
On this page

Also known as body of uterus squamous cell carcinoma

Summary

Squamous cell carcinoma of the corpus uteri (MONDO:0016266) is a cancer. A subtype of squamous cell carcinoma — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Classification: Cancer
  • Prevalence: 1-9 / 1 000 000 (Europe) [Orphanet-validated]

Clinical features

Epidemiology

Prevalence records

23 prevalence record(s), Orphanet, top 20 (validated / broadest geography first):

TypeClassValueGeographyValidation
Annual incidence1-9 / 1 000 0000.12EuropeValidated
Annual incidence<1 / 1 000 0000.039BelgiumValidated
Annual incidence<1 / 1 000 0000.014CroatiaValidated
Annual incidence<1 / 1 000 0000.012FinlandValidated
Annual incidence<1 / 1 000 0000.044GermanyValidated
Annual incidence<1 / 1 000 0000.083IrelandValidated
Annual incidence<1 / 1 000 0000.031MaltaValidated
Annual incidence<1 / 1 000 0000.011NorwayValidated
Annual incidence<1 / 1 000 0000.045PortugalValidated
Annual incidence<1 / 1 000 0000.034SlovakiaValidated
Annual incidence<1 / 1 000 0000.019SloveniaValidated
Annual incidence<1 / 1 000 0000.039SpainValidated
Annual incidence<1 / 1 000 0000.056SwitzerlandValidated
Annual incidence<1 / 1 000 0000.018NetherlandsValidated
Annual incidence<1 / 1 000 0000.041United KingdomValidated
Annual incidence1-9 / 1 000 0000.117AustriaValidated
Annual incidence1-9 / 1 000 0000.12BulgariaValidated
Annual incidence1-9 / 1 000 0000.177Czech RepublicValidated
Annual incidence1-9 / 1 000 0000.139EstoniaValidated
Annual incidence1-9 / 1 000 0000.113ItalyValidated

Identifiers

Disease identifiers

FieldValue
Canonical namesquamous cell carcinoma of the corpus uteri
Mondo IDMONDO:0016266
Orphanet213716
UMLSC4707099
MedGen1633992
GARD0020479
Anatomy (UBERON)UBERON:0009853
Is cancer (heuristic)yes

Also known as: body of uterus squamous cell carcinoma

Disease family

This is a subtype of squamous cell carcinoma. 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 tumorneoplastic disease or syndromeneoplasm › epithelial neoplasm › squamous cell neoplasm › squamous cell carcinomasquamous cell carcinoma of the corpus uteri

Related subtypes (38): bone squamous cell carcinoma, prostate squamous cell carcinoma, trachea squamous cell carcinoma, scrotum squamous cell carcinoma, skin squamous cell carcinoma, bladder squamous cell carcinoma, urethra squamous cell carcinoma, papillary squamous carcinoma, basaloid squamous cell carcinoma, pseudoglandular squamous cell carcinoma, thymus squamous cell carcinoma, ovarian squamous cell carcinoma, renal pelvis squamous cell carcinoma, ureter squamous cell carcinoma, fallopian tube squamous cell carcinoma, squamous carcinoma in situ, keratinizing squamous cell carcinoma, squamous cell lung carcinoma, esophageal squamous cell carcinoma, squamous cell breast carcinoma, adenosquamous carcinoma, cervical squamous cell carcinoma, colorectal squamous cell carcinoma, endometrial squamous cell carcinoma, gallbladder squamous cell carcinoma, gastric squamous cell carcinoma, thyroid gland squamous cell carcinoma, vaginal squamous cell carcinoma, head and neck squamous cell carcinoma, squamous cell carcinoma of penis, squamous cell carcinoma of the small intestine, squamous cell carcinoma of pancreas, squamous cell carcinoma of liver and intrahepatic biliary tract, human papillomavirus-related squamous cell carcinoma, sarcomatoid squamous cell carcinoma, vulvar squamous cell carcinoma, metastatic squamous cell carcinoma, pure squamous carcinoma of the urothelial tract

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.