BC43.10 Familial-genetic hypertrophic cardiomyopathy

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Familial isolated hypertrophic cardiomyopathy is the presence of non-syndromic hypertrophic cardiomyopathy in multiple members of a pedigree, or in the presence of a genetic mutation known to be significantly associated with hypertrophic cardiomyopathy.

synonyms

• Familial-genetic hypertrophic cardiomyopathy
• Familial hypertrophic cardiomyopathy
• Hereditary ventricular hypertrophy
• Hypertrophic cardiomyopathy due to disorder of fatty acid metabolism
• Fatty acid oxidation or ketogenesis disorder with hypertrophic cardiomyopathy
• Hypertrophic cardiomyopathy due to carnitine palmitoyl transferase II deficiency
• Hypertrophic cardiomyopathy due to Carnitine-acylcarnitine translocase deficiency
• Hypertrophic cardiomyopathy due to carnitine deficiency
• Hypertrophic cardiomyopathy due to glycogen storage disease
• Glycogen storage disease with hypertrophic cardiomyopathy
• Hypertrophic cardiomyopathy due to AMP-activated protein kinase deficiency
• Hypertrophic cardiomyopathy due to PRKAG2 syndrome
• Hypertrophic cardiomyopathy due to Pompe disease
• Hypertrophic cardiomyopathy due to glycogen debranching enzyme deficiency
• Hypertrophic cardiomyopathy due to LAMP2 deficiency disease
• Hypertrophic cardiomyopathy due to lysosomal storage disease
• Lysosomal disease with hypertrophic cardiomyopathy
• Hypertrophic cardiomyopathy due to Anderson–Fabry disease
• Hypertrophic cardiomyopathy due to Hurler disease
• Hypertrophic cardiomyopathy due to Hurler disease (MPS I)
• Hypertrophic cardiomyopathy due to mitochondrial disorder
• Mitochondrial disease with hypertrophic cardiomyopathy
• Hypertrophic cardiomyopathy due to MELAS
• Hypertrophic cardiomyopathy due to MELAS - [Mitochondrial Encephalopathy, Lactic acidosis, and Stroke-like episodes]
• Hypertrophic cardiomyopathy due to Friedreich's ataxia
• Other specified familial diseases associated with hypertrophic cardiomyopathy
• Hypertrophic cardiomyopathy due to primary amyloidosis
• Sarcomeric hypertrophic cardiomyopathy
• Syndromic hypertrophic cardiomyopathy
• Hypertrophic cardiomyopathy due to craniofacialcutaneous syndrome
• Hypertrophic cardiomyopathy due to Noonan syndrome
• Hypertrophic cardiomyopathy due to Noonan syndrome with multiple lentigines
• Hypertrophic cardiomyopathy due to LEOPARD syndrome
• Hypertrophic cardiomyopathy due to Costello syndrome
• Hypertrophic cardiomyopathy due to Beckwith–Wiedemann syndrome
• Hypertrophic cardiomyopathy due to Swyer's syndrome
• Hypertrophic cardiomyopathy due to Leprechaunism
• Hypertrophic cardiomyopathy due to Donohue syndrome

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