Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TTN gene.
Comprehensive, easy-to-understand information about this condition
How we create this content →Inheritance patterns describe how genetic conditions are passed from parents to children.
Inheritance patterns describe how genetic conditions are passed from parents to children.
Helpful links for rare disease information and support
Questions that may be helpful when speaking with your healthcare team
Inheritance patterns describe how genetic conditions are passed from parents to children.
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Feb 19, 2026
Online Mendelian Inheritance in Man
AI-Generated Content: This summary was generated using AI. Always consult with qualified healthcare providers for medical guidance.
Organizations with approved therapies for this disease
No approved therapies yet
Research is ongoing — 1 company has orphan drug designations for this disease
Kisho delivers this disease record via API, including phenotypes (HPO), genes, orphan drug designations, screening status, and PAG mapping, with version history and governance.
AI-curated news mentioning hypertrophic cardiomyopathy 9
Updated Feb 18, 2026
New research indicates that cardiac magnetic resonance-derived left atrial strain can effectively restratify patients with hypertrophic cardiomyopathy who are at low risk for sudden cardiac death. This advancement may enhance patient management and risk assessment strategies.
Recent research indicates that serial assessments of myocardial fibrosis can effectively predict clinical outcomes in patients with hypertrophic cardiomyopathy. This finding may enhance patient management strategies and improve prognostic accuracy.
A recent study highlights PRKAG2 cardiac syndrome as a rare condition that can mimic hypertrophic cardiomyopathy in adolescents. This discovery emphasizes the need for accurate diagnosis in patients presenting with unexplained cardiac hypertrophy and conduction system disease.