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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
arrhythmogenic right ventricular cardiomyopathy +  
dilated cardiomyopathy +   
hypertrophic cardiomyopathy +   
A condition in which the myocardium is hypertrophied without an obvious cause. The hypertrophy is generally asymmetric and may be associated with obstruction of the ventricular outflow tract. A form of CARDIAC MUSCLE disease, characterized by left and/or right ventricular hypertrophy (HYPERTROPHY, LEFT VENTRICULAR; HYPERTROPHY, RIGHT VENTRICULAR), frequent asymmetrical involvement of the HEART SEPTUM, and normal or reduced left ventricular volume. Risk factors include HYPERTENSION; AORTIC STENOSIS; and gene MUTATION; (FAMILIAL HYPERTROPHIC CARDIOMYOPATHY).
left ventricular noncompaction +  
myocarditis +   
restrictive cardiomyopathy +   

Synonyms
Exact Synonyms: Asymmetric Septal Hypertrophies ;   Asymmetric Septal Hypertrophy ;   HCM ;   HOCM - Hypertrophic obstructive cardiomyopathy ;   HYPERTR OBSTR CARDIOMYOP ;   Hypertrophic Cardiomyopathies ;   Hypertrophic Obstructive Cardiomyopathies ;   Hypertrophic Obstructive Cardiomyopathy ;   Hypertrophic cardiomyopathy (disorder) ;   Hypertrophic obstructive cardiomyopathy (disorder)
Narrow Synonyms: familial hypertrophic cardiomyopathy
Related Synonyms: HCM - hypertrophic cardiomyopathy
Xrefs: DOID:11984 ;   HP:0001639 ;   ICD10CM:I42.1 ;   ICD10CM:I42.2 ;   ICD9:425.1 ;   ICD9:425.11 ;   ICD9:425.4 ;   MEDGEN:2881 ;   MESH:D002312 ;   MIM:115196
Definition Sources: NCIT:C34449

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