Cecum cancer
diseaseOn this page
Also known as caecum cancercancer of caecummalignant caecum neoplasmmalignant cecum neoplasmmalignant cecum tumormalignant cecum tumourmalignant neoplasm of caecummalignant neoplasm of cecummalignant neoplasm of the cecummalignant tumor of cecummalignant tumor of the cecummalignant tumour of cecummalignant tumour of the cecum
Summary
Cecum cancer (MONDO:0002033) is a cancer. A subtype of cecal neoplasm — 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 | cecum cancer |
| Mondo ID | MONDO:0002033 |
| DOID | DOID:1521 |
| ICD-10-CM | C18.0 |
| ICD-11 | 361612400 |
| NCIT | C9329 |
| UMLS | C0153437 |
| MedGen | 57557 |
| Anatomy (UBERON) | UBERON:0001153 |
| Is cancer (heuristic) | yes |
Also known as: caecum cancer · cancer of caecum · malignant caecum neoplasm · malignant cecum neoplasm · malignant cecum tumor · malignant cecum tumour · malignant neoplasm of caecum · malignant neoplasm of cecum · malignant neoplasm of the cecum · malignant tumor of cecum · malignant tumor of the cecum · malignant tumour of cecum · malignant tumour of the cecum
Disease family
An umbrella term covering 3 Mondo subtypes.
Classification path: disease › human disease › disease by body system or component › digestive system disorder › intestinal disorder › large intestine disorder › colonic disorder › cecal disorder › cecal neoplasm › cecum cancer
Related subtypes (4): cecum villous adenoma, appendiceal neoplasm, cecum neuroendocrine tumor G1, benign neoplasm of cecum
Subtypes (3): appendix cancer, cecum lymphoma, cecum carcinoma
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.