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Ontology Browser
Term:
Muscular Dystrophy, Cardiac Type (DOID:9005305)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
cardiomyopathy +     
muscular dystrophy +     
Adult-Onset Muscular Dystrophy with Leukoencephalopathy 
alcoholic cardiomyopathy  
Alpha-B Crystallinopathy with Cataract 
Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis 
Ataxia, Deafness, and Cardiomyopathy 
Atrial Dilation and Standstill +   
autosomal recessive limb-girdle muscular dystrophy type 2D  
Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts 
Bassoe Syndrome 
Becker muscular dystrophy +   
Cardiomyopathy Associated with Myopathy and Sudden Death 
Cardiomyopathy Hypogonadism Collagenoma Syndrome 
Cardioneuromyopathy with Hyaline Masses and Nemaline Rods 
Chagas Cardiomyopathy  
Congenital Infantile Muscular Dystrophy with Cataract and Hypogonadism 
congenital muscular dystrophy +   
Danon disease  
Diabetic Cardiomyopathies  
distal myopathy +   
Duchenne muscular dystrophy +   
Early-Onset Myopathy with Fatal Cardiomyopathy  
Emery-Dreifuss muscular dystrophy +   
endocardial fibroelastosis +   
endomyocardial fibrosis  
extrinsic cardiomyopathy +   
facioscapulohumeral muscular dystrophy +   
Familial Cardiac Lipidosis 
Fatal Fetal Cardiomyopathy due to Myocardial Calcification 
glycogen storage disease VII  
Hypertaurinuric Cardiomyopathy 
intrinsic cardiomyopathy +   
Kearns-Sayre syndrome  
Keshan disease  
limb-girdle muscular dystrophy +   
linear skin defects with multiple congenital anomalies 3  
Mitochondrial Cardiomyopathy  
mitochondrial DNA depletion syndrome 12a  
mitochondrial DNA depletion syndrome 12b  
Muscular Dystrophy, Animal +   
Muscular Dystrophy, Barnes Type 
Muscular Dystrophy, Cardiac Type 
Muscular Dystrophy, Mabry Type 
Muscular Dystrophy, Pseudohypertrophic, with Internalized Capillaries 
Myocardial Reperfusion Injury  
myocarditis +   
myofibrillar myopathy 2  
Myofibrillar Myopathy, ZASP-Related  
Myopathy with Abnormal Lipid Metabolism  
MYOPATHY, SCAPULOHUMEROPERONEAL  
myotonic disease +   
oculopharyngeal muscular dystrophy +   
Oculopharyngodistal Myopathy +   
Progressive Muscular Dystrophy, Pectorodorsal 
Roifman Syndrome  
scapuloperoneal myopathy +   
Sengers syndrome  
systemic primary carnitine deficiency disease  
Uruguay faciocardiomusculoskeletal syndrome  
Vacuolar Neuromyopathy 

Synonyms
Primary IDs: MESH:C563247
Alternate IDs: OMIM:309930 ;   RDO:0012575

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