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cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction (CMH23) - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction

MONDO:0800347

Also known as:CMH23

Overview

Diagnosis

Biomarker and diagnostic research for cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction 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 cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction.

200 publications have been identified in PubMed for cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction. Research spans Case Report / Case Series (36%), Review / Meta-Analysis (22%), and Basic Science / Preclinical (16%).

Research Type	Count	% of Total
Patient case studies	62	36%

Data assembled from 2 of 12 sources · Last updated Sep 20, 2026, 5:40 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

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cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction

Overview

Diagnosis

Research Landscape

Medical References

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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