colon neuroendocrine tumor G1

disease
On this page

Also known as carcinoid tumor of coloncarcinoid tumor of the coloncarcinoid tumour of coloncarcinoid tumour of the coloncolon carcinoid tumorcolon carcinoid tumor (disease)colon carcinoid tumourcolon carcinoid tumour (disease)colon NET G1colon neuroendocrine neoplasm G1colon neuroendocrine tumor, well differentiated, low gradecolonic carcinoid tumorcolonic carcinoid tumourgrade 1 neuroendocrine neoplasm of colon

Summary

colon neuroendocrine tumor G1 (MONDO:0006155) is a cancer and 1 clinical trial. A subtype of colorectal neuroendocrine tumor G1 — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Classification: Cancer
  • Clinical trials: 1

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namecolon neuroendocrine tumor G1
Mondo IDMONDO:0006155
EFOEFO:1000188
NCITC5497
UMLSC1333084
MedGen234158
GARD0024313
Anatomy (UBERON)UBERON:0001155
Is cancer (heuristic)yes

Also known as: carcinoid tumor of colon · carcinoid tumor of the colon · carcinoid tumour of colon · carcinoid tumour of the colon · colon carcinoid tumor · colon carcinoid tumor (disease) · colon carcinoid tumour · colon carcinoid tumour (disease) · colon NET G1 · colon neuroendocrine neoplasm G1 · colon neuroendocrine tumor G1 · colon neuroendocrine tumor, well differentiated, low grade · colonic carcinoid tumor · colonic carcinoid tumour · grade 1 neuroendocrine neoplasm of colon

Disease family

This is a subtype of colorectal neuroendocrine tumor G1. 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 › digestive system disorderintestinal disorderintestinal neoplasmcolorectal neoplasmcolorectal neuroendocrine tumor G1colon neuroendocrine tumor G1

Related subtypes (1): rectal neuroendocrine tumor G1

Subtypes (4): ascending colon neuroendocrine tumor G1, cecum neuroendocrine tumor G1, ileal neuroendocrine tumor G1, jejunal neuroendocrine tumor G1

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: 1.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT04907643Not specifiedRECRUITINGVirtual Reality for GI Cancer Pain to Improve Patient Reported Outcomes

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