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

Rare Disease

cecum neuroendocrine tumor G1

MONDO:0006126

Also known as:caecal carcinoid tumorcaecal carcinoid tumourcaecum NET G1

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Overview

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

Clinical Trials3 registered · 1 recruiting

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.

3 clinical trials registered, 1 recruiting. Interventions under study include drug therapy and medical devices. Pipeline includes 1 PHASE3, 1 PHASE2, 1 NA. Research is sponsored by a mix of industry and academic institutions.

10 publications have been identified in PubMed for cecum neuroendocrine tumor G1. Research spans Case Report / Case Series (50%), Epidemiology / Natural History (30%), and Review / Meta-Analysis (20%).

Research Type	Count	% of Total
Patient case studies	5

Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 8:43 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

Questions for Your Care Team

→Are any of the 3 active clinical trials a good fit for my situation?
→Are there specialists or centers of excellence for this condition in my area?
→Is there a patient registry I should consider joining?

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cecum neuroendocrine tumor G1

Overview

Research Landscape

Medical References

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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