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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Cardiomegaly +     
arrhythmogenic biventricular cardiomyopathy 
arrhythmogenic left ventricular cardiomyopathy 
arrhythmogenic right ventricular cardiomyopathy +   
Biventricular Hypertrophy 
dilated cardiomyopathy +   
An intrinsic cardiomyopathy that is characterized by an an enlarged heart and damage to the myocardium causing the heart to pump blood inefficiently. (DO)
Ethanolaminosis 
geleophysic dysplasia +   
hypertrichotic osteochondrodysplasia Cantu type  
hypertrophic cardiomyopathy +   
infantile histiocytoid cardiomyopathy  
Left Ventricular Hypertrophy +   
left ventricular noncompaction +   
long QT syndrome +   
restrictive cardiomyopathy +   
Right Ventricular Hypertrophy +   

Synonyms
Exact Synonyms: congestive cardiomyopathies ;   congestive cardiomyopathy ;   dilated cardiomyopathies ;   idiopathic dilated cardiomyopathies
Narrow Synonyms: ANKRD1-related dilated cardiomyopathy ;   FDC ;   IDCM ;   LVNC4 ;   NEONATAL CARDIOMYOPATHY ;   autosomal dominant dilated cardiomyopathy ;   dilated cardiomyopathy, and heart failure ;   dilated cardiomyopathy, autosomal recessive ;   dilated cardiomyopathy, dominant ;   dilated cardiomyopathy, recessive ;   familial dilated cardiomyopathy ;   familial idiopathic cardiomyopathies ;   familial idiopathic cardiomyopathy ;   fatal cardiomyopathy ;   fatal cardiomyopathy, infantile ;   idiopathic dilated cardiomyopathy ;   idiopathic dilation cardiomyopathy ;   left ventricular noncompaction 4 ;   primary dilated cardiomyopathy
Related Synonyms: ANKRD1-related condition
Primary IDs: MESH:D002311
Xrefs: EFO:0000372 ;   EFO:0000407 ;   EFO:0009094 ;   EFO:0009142 ;   EFO:0010953 ;   GARD:221 ;   MIM:PS115200 ;   NCI:C84673 ;   ORDO:217604
Definition Sources: http://en.wikipedia.org/wiki/Dilated_cardiomyopathy "DO" "DO"

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