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

Rare Disease

small intestinal neuroendocrine tumor G1

MONDO:0000540

Also known as:carcinoid tumor of small bowelcarcinoid tumor of small intestinecarcinoid tumor of the small bowel

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Overview

A well differentiated, low grade neuroendocrine tumor (carcinoid tumor) that arises from the small intestine. 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 · 1 recruiting

Diagnosis

Biomarker and diagnostic research for small intestinal 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, 1 recruiting. Interventions under study include medical devices. Pipeline includes 1 NA. Research is primarily sponsored by academic and government institutions.

57 publications have been identified in PubMed for small intestinal neuroendocrine tumor G1. Research spans Case Report / Case Series (32%), Diagnostic / Biomarker (19%), and Review / Meta-Analysis (16%).

Research Type	Count	% of Total
Patient case studies	18

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 4:41 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

Questions for Your Care Team

→Are any of the 1 active clinical trial 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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small intestinal 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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