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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
acquired night blindness 
acute hemorrhagic conjunctivitis 
alcoholic cardiomyopathy  
Ataxia, Deafness, and Cardiomyopathy 
Atrial Dilation and Standstill +   
autosomal recessive limb-girdle muscular dystrophy type 2D  
Avitaminosis +   
Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts 
biotin deficiency 
Cardiomyopathy Associated with Myopathy and Sudden Death 
Cardiomyopathy Hypogonadism Collagenoma Syndrome 
Cardioneuromyopathy with Hyaline Masses and Nemaline Rods 
Chagas Cardiomyopathy  
copper deficiency myelopathy 
Coxsackievirus Infections +   
Danon disease  
Diabetic Cardiomyopathies  
Early-Onset Myopathy with Fatal Cardiomyopathy  
Echovirus Infections +   
Encephalomyelitis, Enzootic Porcine 
endemic goiter 
endocardial fibroelastosis +   
endomyocardial fibrosis  
extrinsic cardiomyopathy +   
Familial Cardiac Lipidosis 
Fatal Fetal Cardiomyopathy due to Myocardial Calcification 
folic acid deficiency anemia +   
hepatitis A  
Hypertaurinuric Cardiomyopathy 
infantile histiocytoid cardiomyopathy  
intrinsic cardiomyopathy +   
iron deficiency anemia +   
Kearns-Sayre syndrome  
Keshan disease  
A nutritional deficiency that is disease characterized by a cardiomyopathy secondary to selenium deficiency. (DO)
linear skin defects with multiple congenital anomalies 3  
Mitochondrial Cardiomyopathy  
mitochondrial DNA depletion syndrome 12a  
mitochondrial DNA depletion syndrome 12b  
Muscular Dystrophy, Cardiac Type 
Myocardial Reperfusion Injury  
myocarditis +   
myofibrillar myopathy 2  
pernicious anemia +   
poliomyelitis +   
Potassium Deficiency  
primary hypomagnesemia +   
Protein Deficiency +   
protein-energy malnutrition +   
pyridoxine deficiency anemia  
riboflavin deficiency  
Roifman Syndrome  
Sengers syndrome  
Swine Vesicular Disease 
systemic primary carnitine deficiency disease  
Uruguay Faciocardiomusculoskeletal Syndrome  
Zinc Deficiency +   

Synonyms
Primary IDs: MESH:C536166 ;   RDO:0001632
Xrefs: GARD:8761
Definition Sources: https://en.wikipedia.org/wiki/Keshan_disease "DO"

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.