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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Apical Hypertrophic Cardiomyopathy +   
autosomal dominant nonsyndromic deafness 22  
endomyocardial fibrosis  
FAMILIAL HYPERTROPHIC CARDIOMYOPATHY 19  
FAMILIAL HYPERTROPHIC CARDIOMYOPATHY 30, ATRIAL  
Familial Restrictive Cardiomyopathy 6  
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  
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the FLNC gene on chromosome 7q32. (DO)
Hypertrophic Cardiomyopathy 27  
Hypertrophic Cardiomyopathy 28  
Hypertrophic Cardiomyopathy 29  
hypertrophic cardiomyopathy 3  
hypertrophic cardiomyopathy 4  
hypertrophic cardiomyopathy 6  
hypertrophic cardiomyopathy 7  
hypertrophic cardiomyopathy 8  
hypertrophic cardiomyopathy 9  
Loeffler endocarditis 
restrictive cardiomyopathy 1  
restrictive cardiomyopathy 2 
restrictive cardiomyopathy 3  

Synonyms
Exact Synonyms: CMH26 ;   familial hypertrophic cardiomyopathy 26
Related Synonyms: ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 15 ;   ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 15 ;   ARVC15 ;   ARVD15 ;   CARDIOMYOPATHY, DILATED, 1PP ;   CMD1PP ;   RCM5 ;   familial restrictive cardiomyopathy 5
Primary IDs: OMIM:617047
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/25351925 "DO" "DO"

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