appendix neuroendocrine tumor G1

disease

On this page

Also known as appendiceal carcinoid tumorappendiceal carcinoid tumourappendix carcinoid endocrine tumourappendix carcinoid tumorappendix carcinoid tumourappendix NET G1appendix NET G1 (carcinoid)appendix neuroendocrine tumor G1 (carcinoid)appendix neuroendocrine tumour G1 (carcinoid)carcinoid tumor of appendixcarcinoid tumor of the appendixcarcinoid tumour of appendixcarcinoid tumour of the appendixgrade 1 neuroendocrine neoplasm of vermiform appendixvermiform appendix carcinoid tumorvermiform appendix carcinoid tumor (disease)vermiform appendix carcinoid tumourvermiform appendix carcinoid tumour (disease)vermiform appendix NET G1vermiform appendix neuroendocrine neoplasm G1

Summary

appendix neuroendocrine tumor G1 (MONDO:0006091) is a cancer and 1 clinical trial. A subtype of cecum 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

Field	Value
Canonical name	appendix neuroendocrine tumor G1
Mondo ID	MONDO:0006091
EFO	EFO:1000092
DOID	DOID:0050911
NCIT	C4138
SNOMED CT	253002004
UMLS	C0334298
MedGen	90758
GARD	0024288
Anatomy (UBERON)	UBERON:0001154
Is cancer (heuristic)	yes

Also known as: appendiceal carcinoid tumor · appendiceal carcinoid tumour · appendix carcinoid endocrine tumour · appendix carcinoid tumor · appendix carcinoid tumour · appendix NET G1 · appendix NET G1 (carcinoid) · appendix neuroendocrine tumor G1 (carcinoid) · appendix neuroendocrine tumour G1 (carcinoid) · carcinoid tumor of appendix · carcinoid tumor of the appendix · carcinoid tumour of appendix · carcinoid tumour of the appendix · grade 1 neuroendocrine neoplasm of vermiform appendix · vermiform appendix carcinoid tumor · vermiform appendix carcinoid tumor (disease) · vermiform appendix carcinoid tumour · vermiform appendix carcinoid tumour (disease) · vermiform appendix NET G1 · vermiform appendix neuroendocrine neoplasm G1 (+1 more)

Disease family

This is a subtype of cecum 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 disorder › intestinal disorder › large intestine disorder › colonic disorder › cecal disorder › cecal neoplasm › cecum neuroendocrine tumor G1 › appendix 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)

Phase	Trials
Not specified	1

Top trials by phase / activity

NCT	Phase	Status	Title
NCT05734430	Not specified	RECRUITING	Genetics of Appendix Cancer Study

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