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subependymoma - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

subependymoma

MONDO:0007667

Also known as:SUBEPENDYMOMA, benignWHO grade I ependymal neoplasmWHO grade I ependymal tumor

Overview

Subependymoma is a rare and slow growing type of ependymoma, often presenting in middle-aged adults, found more commonly in men than in women, usually located in the fourth and lateral ventricles and manifesting with variable symptoms including headache, nausea, and loss of balance. In some cases it can be asymptomatic. It is usually associated with a better prognosis than other forms of ependymoma.

Diagnosis

Biomarker and diagnostic research for subependymoma 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.

No clinical trials have been registered for subependymoma.

39 publications have been identified in PubMed for subependymoma. Research spans Case Report / Case Series (26%), Review / Meta-Analysis (23%), and Clinical Trial Publication (21%).

Research Type	Count	% of Total
Patient case studies	10	26%

Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 3:56 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:251639

GARD

Genetic and Rare Diseases Info Center

GARD:10070

Questions for Your Care Team

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subependymoma

Overview

Diagnosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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