ascending colon neuroendocrine tumor G1

disease
On this page

Also known as ascending colon carcinoid tumorascending colon carcinoid tumor (disease)ascending colon carcinoid tumourascending colon carcinoid tumour (disease)ascending colon NET G1ascending colon neuroendocrine neoplasm G1ascending colon neuroendocrine tumor, well differentiated, low gradecarcinoid tumor of ascending coloncarcinoid tumor of the ascending coloncarcinoid tumour of ascending coloncarcinoid tumour of the ascending colongrade 1 neuroendocrine neoplasm of ascending colon

Summary

ascending colon neuroendocrine tumor G1 (MONDO:0006093) is a cancer. A subtype of colon neuroendocrine tumor G1 — 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 nameascending colon neuroendocrine tumor G1
Mondo IDMONDO:0006093
NCITC6427
UMLSC1332340
MedGen231386
GARD0024290
Anatomy (UBERON)UBERON:0001156
Is cancer (heuristic)yes

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

Disease family

This is a subtype of colon 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 G1ascending colon neuroendocrine tumor G1

Related subtypes (3): 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: 0.

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