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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Apical Hypertrophic Cardiomyopathy +   
autosomal dominant nonsyndromic deafness 22  
FAMILIAL HYPERTROPHIC CARDIOMYOPATHY 19  
FAMILIAL HYPERTROPHIC CARDIOMYOPATHY 30, ATRIAL  
hypertrophic cardiomyopathy 1  
hypertrophic cardiomyopathy 10  
hypertrophic cardiomyopathy 11  
hypertrophic cardiomyopathy 12  
hypertrophic cardiomyopathy 13  
hypertrophic cardiomyopathy 14  
hypertrophic cardiomyopathy 15  
hypertrophic cardiomyopathy 16  
hypertrophic cardiomyopathy 17  
hypertrophic cardiomyopathy 18  
hypertrophic cardiomyopathy 2  
hypertrophic cardiomyopathy 20  
hypertrophic cardiomyopathy 21  
hypertrophic cardiomyopathy 25  
hypertrophic cardiomyopathy 26  
Hypertrophic Cardiomyopathy 27  
Hypertrophic Cardiomyopathy 28  
Hypertrophic Cardiomyopathy 29  
A disease characterized by recurrent syncope, dyspnea on exertion, and palpitations. Caused by homozygous mutation in the KLHL24 gene on chromosome 3q27.
hypertrophic cardiomyopathy 3  
hypertrophic cardiomyopathy 4  
hypertrophic cardiomyopathy 6  
hypertrophic cardiomyopathy 7  
hypertrophic cardiomyopathy 8  
hypertrophic cardiomyopathy 9  

Synonyms
Exact Synonyms: CMH29 ;   familial hypertrophic cardiomyopathy 29, with polyglucosan bodies
Primary IDs: OMIM:620236
Definition Sources: OMIM:620236

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