Ontology Browser

Term:
mitochondrial encephalomyopathy (DOID:890)
Annotations: Rat: (43) Mouse: (44) Human: (60) Chinchilla: (34) Bonobo: (34) Dog: (42) Squirrel: (34)
Parent Terms Term With Siblings Child Terms
Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts 
central pontine myelinolysis  
chronic progressive external ophthalmoplegia +   
Combined Oxidative Phosphorylation Deficiency 3  
Encephalopathy with Intracranial Calcification, Growth Hormone Deficiency, Microcephaly, and Retinal Degeneration 
Episodic Mitochondrial Myopathy with or without Optic Atrophy and Reversible Leukoencephalopathy  
Ethanolaminosis 
Glutaric Acidemia I  
GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE  
hepatic encephalopathy +   
INFLAMMATORY BOWEL DISEASE, IMMUNODEFICIENCY, AND ENCEPHALOPATHY  
kernicterus +   
Marchiafava-Bignami Disease 
Metabolic Brain Diseases, Inborn +   
METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION  
mitochondrial DNA depletion syndrome 11  
mitochondrial DNA depletion syndrome 12a  
mitochondrial DNA depletion syndrome 12b  
mitochondrial DNA depletion syndrome 14  
mitochondrial DNA depletion syndrome 15  
Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form, Autosomal Recessive +   
mitochondrial encephalomyopathy +   
A heterogenous group of disorders characterized by alterations of mitochondrial metabolism that result in muscle and nervous system dysfunction. These are often multisystemic and vary considerably in age at onset (usually in the first or second decade of life), distribution of affected muscles, severity, and course. (From Adams et al., Principles of Neurology, 6th ed, pp984-5)
Mitochondrial Myopathy with a Defect in Mitochondrial Protein Transport 
Mitochondrial Myopathy with Diabetes 
Mitochondrial Myopathy with Lactic Acidosis  
Mitochondrial Myopathy, and Ataxia  
Mitochondrial Myopathy, Infantile, Transient  
Mitochondrial Myopathy, Lethal Infantile  
Mitochondrial Progressive Myopathy with Congenital Cataract, Hearing Loss, and Developmental Delay  
MYOPATHY, ISOLATED MITOCHONDRIAL, AUTOSOMAL DOMINANT  
Neuropathy Ataxia and Retinitis Pigmentosa  
Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency  
Reye syndrome  
Schofer Beetz Bohl Syndrome 
Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type)  
Trifunctional Protein Deficiency with Myopathy and Neuropathy  
Wernicke encephalopathy  

Synonyms
Exact Synonyms: mitochondrial encephalomyopathies
Narrow Synonyms: ENCEPHALOCARDIOMYOPATHY, MITOCHONDRIAL
Primary IDs: MESH:D017237 ;   RDO:0003323
Definition Sources: MESH:D017237

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