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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  
hypertrophic cardiomyopathy 3  
hypertrophic cardiomyopathy 4  
hypertrophic cardiomyopathy 6  
hypertrophic cardiomyopathy 7  
hypertrophic cardiomyopathy 8  
A familial hypertrophic cardiomyopathy that has_material_basis_in homozygous or heterozygous mutation in the MYL3 gene. (DO)
hypertrophic cardiomyopathy 9  

Synonyms
Exact Synonyms: CMH8 ;   cardiomyopathy hypertrophic mid-left ventricular chamber type 1 ;   cardiomyopathy, familial hypertrophic, 8
Primary IDs: MESH:C563866 ;   RDO:0013011
Alternate IDs: OMIM:608751
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/8673105 "DO" "DO"

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