ICD-11 code : BC43.10;
Preferred Label : Familial-genetic hypertrophic cardiomyopathy;
ICD-11 definition : Familial isolated hypertrophic cardiomyopathy is the hereditary, nonsyndromic form
of hypertrophic cardiomyopathy (HCM), a primary cardiac disease characterized by an
asymmetrical hypertrophy of the left ventricle. The symptoms include dyspnea, syncope,
collapse, palpitations, and chest pain. They can be readily provoked by exercise.
The disease often leads to a slight-to-moderate invalidation and carries a high incidence
of sudden death, usually caused by ventricular tachyarrythmia.;
ICD-11 synonym : Familial hypertrophic cardiomyopathy;
Origin ID : 1408928442;
Currated CISMeF NLP mapping
Familial isolated hypertrophic cardiomyopathy is the hereditary, nonsyndromic form
of hypertrophic cardiomyopathy (HCM), a primary cardiac disease characterized by an
asymmetrical hypertrophy of the left ventricle. The symptoms include dyspnea, syncope,
collapse, palpitations, and chest pain. They can be readily provoked by exercise.
The disease often leads to a slight-to-moderate invalidation and carries a high incidence
of sudden death, usually caused by ventricular tachyarrythmia.
