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appendix neuroendocrine tumor G1 - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

appendix neuroendocrine tumor G1

MONDO:0006091

Also known as:appendiceal carcinoid tumorappendiceal carcinoid tumourappendix NET G1

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Overview

A well differentiated, low grade tumor with neuroendocrine differentiation that arises from the appendix. The mitotic count is less than 2 per 10 HPF and/or the Ki67 index is equal to or less than 2 percent.

Clinical Trials1 registered

Diagnosis

Biomarker and diagnostic research for appendix neuroendocrine tumor G1 has been reported in the published literature.

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

1 clinical trial registered. Interventions under study include other interventions and gene therapy. Research is primarily sponsored by academic and government institutions.

14 publications have been identified in PubMed for appendix neuroendocrine tumor G1. Research spans Case Report / Case Series (50%), Epidemiology / Natural History (21%), and Review / Meta-Analysis (14%).

Research Type	Count	% of Total
Patient case studies	7	50%

Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 2:55 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

Questions for Your Care Team

→Are any of the 1 active clinical trial a good fit for my situation?
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appendix neuroendocrine tumor G1

Overview

Diagnosis

Research Landscape

Medical References

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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