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Ontology Browser

Term:
Mitochondrial Myopathy with Diabetes (DOID:9002482)
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Parent Terms Term With Siblings Child Terms
diabetes mellitus +     
Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus 
chronic progressive external ophthalmoplegia +   
Combined Cerebellar and Peripheral Ataxia with Hearing Loss and Diabetes Mellitus  
combined oxidative phosphorylation deficiency 3  
Congenital Heart Defects, and Other Congenital Anomalies  
Diabetes Complications +   
Diabetes Mellitus, Congenital Autoimmune 
Diabetes Mellitus, Experimental   
Diabetes Mellitus, New-Onset after Transplantation  
Donohue syndrome  
Episodic Mitochondrial Myopathy with or without Optic Atrophy and Reversible Leukoencephalopathy  
Feigenbaum Bergeron Richardson Syndrome 
Furukawa Takagi Nakao Syndrome 
gestational diabetes +   
Herrmann Syndrome 
Hyperproinsulinemia  
Insulin-Resistant Diabetes Mellitus, with Acanthosis Nigricans  
Latent Autoimmune Diabetes in Adults  
Lipoatrophy with Diabetes, Hepatic Steatosis, Cardiomyopathy, and Leukomelanodermic Papules 
Lymphedema-Distichiasis Syndrome with Renal Disease and Diabetes Mellitus  
Martinez-Frias Syndrome 
Microcephaly, Epilepsy, and Diabetes Syndrome  
Mitchell-Riley Syndrome  
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 +   
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  
Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus 
MYOPATHY, ISOLATED MITOCHONDRIAL, AUTOSOMAL DOMINANT  
NARP syndrome  
neonatal diabetes mellitus +   
PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES  
prediabetes syndrome  
Premature Aging, Okamoto Type 
Premature Atherosclerosis with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease 
thiamine-responsive megaloblastic anemia syndrome  
type 1 diabetes mellitus +   
type 2 diabetes mellitus +   
Wolfram syndrome, mitochondrial form 
Woodhouse-Sakati Syndrome  
Yorifuji Okuno Syndrome 

Synonyms
Exact Synonyms: Mitochondrial Myopathy, Lipid Type
Primary IDs: MESH:C564026 ;   RDO:0013128

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