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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  
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the CSRP3 gene on chromosome 11p15. (DO)
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  
hypertrophic cardiomyopathy 9  

Synonyms
Exact Synonyms: CMH12 ;   cardiomyopathy familial hypertrophic 12
Broad Synonyms: CSRP3-RELATED DISORDER
Primary IDs: OMIM:612124
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/12642359 "DO" "DO"

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