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Hypertrophic cardiomyopathy
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Enlargement of the heart muscle
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Subclasses 5
Influences rating
Costello syndrome
Medical condition
Fabry disease
Rare human genetic lysosomal storage disorder
Myotonic dystrophy
Disorder in which muscles fail to relax
Hunter syndrome
X-linked recessive genetic condition
familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy caused by mutations in the genes encoding components of the sarcomere, in the absence of predisposing conditions
Subject of 13
Genetic Studies of Hypertrophic Cardiomyopathy in Singaporeans Identify Variants in TNNI3 and TNNT2 that Are Common in Chinese Patients
scientific article published on 20 August 2020
Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing
scientific article published on 8 February 2013
Wearable cardioverter-defibrillator as bridging to ICD in pediatric hypertrophic cardiomyopathy with myocardial bridging - a case report
scientific article published on 11 May 2020
Usefulness and Safety of Transcatheter Ablation of Atrial Fibrillation in Patients With Hypertrophic Cardiomyopathy
Appropriate and inappropriate shocks in hypertrophic cardiomyopathy patients with subcutaneous implantable cardioverter-defibrillators: An international multicenter study
scientific article published on 18 February 2020
Changes in left atrial function, left ventricle remodeling, and fibrosis after septal myectomy for obstructive hypertrophic cardiomyopathy
scientific article published on 08 July 2020
In-Hospital Postoperative Atrial Fibrillation Indicates a Poorer Clinical Outcome after Myectomy for Obstructive Hypertrophic Cardiomyopathy
scientific article published on 04 October 2019
Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy
scientific article
Exercise capacity and paroxysmal atrial fibrillation in patients with hypertrophic cardiomyopathy
scientific article published on December 10, 2013
Prevalence and distribution of sarcomeric gene mutations in Japanese patients with familial hypertrophic cardiomyopathy
scientific article published on 23 November 2011
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Wikipedia

Hypertrophic cardiomyopathy (HCM, or HOCM when obstructive) is a condition in which muscle tissues of the heart become thickened without an obvious cause. The parts of the heart most commonly affected are the interventricular septum and the ventricles. This results in the heart being less able to pump blood effectively and also may cause...

Instance of
designated intractable/rare disease
Rare disease
class of disease
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Disease
References
Wikidata