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cardiomyopathy, dilated, 1QQ - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

cardiomyopathy, dilated, 1QQ

MONDO:0979239

Overview

GeneticsAutosomal dominant

Clinical Presentation

Built from Human Phenotype Ontology (HPO) phenotype annotations and GeneReviews clinical descriptions. Features represent findings documented across known cases — not an exhaustive list of possible symptoms.

Features include always present findings: Enlarged and weakened heart (dilated cardiomyopathy) and Elevated left ventricular end-diastolic diameter; and common findings: Mildly reduced left ventricular ejection fraction and Left ventricular noncompaction cardiomyopathy. 5 total HPO annotations.

Organ System	Phenotype Count	Example Features
Heart and blood vessels	5	Mildly reduced left ventricular ejection fraction, Left ventricular noncompaction cardiomyopathy, Severely reduced left ventricular ejection fraction

Prognosis

Phenotype severity distribution: 2 always present features, 2 common features.

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 11:54 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:621251

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cardiomyopathy, dilated, 1QQ

Overview

Clinical Presentation

Prognosis

Medical References

External Resources

OMIM

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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