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Ontology Browser

Term:
Mitochondrial Cardiomyopathy (DOID:9000777)
Annotations: Rat: (4) Mouse: (5) Human: (5) Chinchilla: (3) Bonobo: (3) Dog: (4) Squirrel: (3) Pig: (4)
Parent Terms Term With Siblings Child Terms
3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency  
adult-onset ataxia and polyneuropathy  
alcoholic cardiomyopathy  
Ataxia Neuropathy Spectrum  
Ataxia, Deafness, and Cardiomyopathy 
Atrial Dilation and Standstill +   
autosomal recessive limb-girdle muscular dystrophy type 2D  
Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts 
Bjornstad syndrome  
carbamoyl phosphate synthetase I deficiency disease  
Cardiomyopathy Associated with Myopathy and Sudden Death 
Cardiomyopathy Hypogonadism Collagenoma Syndrome 
Cardioneuromyopathy with Hyaline Masses and Nemaline Rods 
Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal  
Chagas Cardiomyopathy  
Childhood Myocerebrohepatopathy Spectrum 
coenzyme Q10 deficiency disease +   
combined oxidative phosphorylation deficiency +   
Cowden-Like Syndrome  
cytochrome-c oxidase deficiency disease +   
Danon disease  
deafness-dystonia-optic neuronopathy syndrome  
Deoxyguanosine Kinase Deficiency  
Diabetic Cardiomyopathies  
early infantile epileptic encephalopathy 39  
Early-Onset Myopathy with Fatal Cardiomyopathy  
encephalopathy due to defective mitochondrial and peroxisomal fission 1  
ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2  
endocardial fibroelastosis +   
endomyocardial fibrosis  
ethylmalonic encephalopathy  
extrinsic cardiomyopathy +   
Familial Cardiac Lipidosis 
Fatal Fetal Cardiomyopathy due to Myocardial Calcification 
Friedreich ataxia +   
GRACILE syndrome  
Hypermetabolism due to Defect in Mitochondria 
Hypertaurinuric Cardiomyopathy 
hypomyelinating leukodystrophy 4  
hypotonia-cystinuria syndrome  
infantile histiocytoid cardiomyopathy  
intrinsic cardiomyopathy +   
Kearns-Sayre syndrome  
Keshan disease  
Late-Onset Carnitine Palmitoyltransferase II Deficiency  
Leber hereditary optic neuropathy +   
Leigh disease +   
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation  
linear skin defects with multiple congenital anomalies 3  
Medium Chain 3-Ketoacyl-CoA Thiolase Deficiency 
Mitochondrial Cardiomyopathy  
A group of diseases in which the dominant feature is the involvement of the cardiac muscle, associated with abnormal mitochondria function.
mitochondrial complex I deficiency +   
mitochondrial complex II deficiency  
mitochondrial complex III deficiency +   
mitochondrial complex V (ATP synthase) deficiency +   
Mitochondrial Cytopathy +   
mitochondrial DNA depletion syndrome +   
mitochondrial DNA depletion syndrome 12a  
mitochondrial DNA depletion syndrome 12b  
Mitochondrial Phosphate Carrier Deficiency  
mitochondrial pyruvate carrier deficiency  
multiple acyl-CoA dehydrogenase deficiency +   
multiple mitochondrial dysfunctions syndrome +   
Muscular Dystrophy, Cardiac Type 
Myocardial Reperfusion Injury  
myocarditis +   
myofibrillar myopathy 2  
Myopathy with Giant Abnormal Mitochondria 
Myopathy, Cataract, Hypogonadism Syndrome 
Noninsulin-Dependent Diabetes Mellitus with Deafness  
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria 
optic atrophy 1  
Parkinson's Disease, Mitochondrial  
Pearson syndrome  
Progressive External Ophthalmoplegia with Hypogonadism 
Proximal Myopathy with Focal Depletion of Mitochondria 
pyruvate carboxylase deficiency disease +   
pyruvate decarboxylase deficiency +   
Roifman Syndrome  
Sarcosinemia  
Sengers syndrome  
sensory ataxic neuropathy, dysarthria, and ophthalmoparesis  
Spinocerebellar Ataxia with Epilepsy  
Succinate-Coa Ligase Deficiency +   
systemic primary carnitine deficiency disease  
Uruguay Faciocardiomusculoskeletal Syndrome  
VDAC Deficiency 
very long chain acyl-CoA dehydrogenase deficiency  
Wolfram syndrome 2  

Synonyms
Exact Synonyms: Mitochondrial cardiomyopathies
Narrow Synonyms: EXERCISE INTOLERANCE, CARDIOMYOPATHY, AND SEPTOOPTIC DYSPLASIA
Primary IDs: RDO:9000719

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