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Ontology Browser

Term:
Mitochondrial DNA Depletion Syndrome, MNGIE Type (DOID:9001263)
Annotations: Rat: (5) Mouse: (8) Human: (8) Chinchilla: (6) Bonobo: (6) Dog: (5) Squirrel: (6) Pig: (5)
Parent Terms Term With Siblings Child Terms
Alpers-Huttenlocher syndrome +   
mitochondrial DNA depletion syndrome 11  
mitochondrial DNA depletion syndrome 12a  
mitochondrial DNA depletion syndrome 12b  
mitochondrial DNA depletion syndrome 13  
mitochondrial DNA depletion syndrome 14  
mitochondrial DNA depletion syndrome 15  
Mitochondrial DNA Depletion Syndrome 16  
Mitochondrial DNA Depletion Syndrome 17  
Mitochondrial DNA Depletion Syndrome 18  
mitochondrial DNA depletion syndrome 2  
mitochondrial DNA depletion syndrome 3  
mitochondrial DNA depletion syndrome 5  
mitochondrial DNA depletion syndrome 6  
mitochondrial DNA depletion syndrome 8b  
mitochondrial DNA depletion syndrome 9  
Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form, Autosomal Recessive +   
Mitochondrial DNA Depletion Syndrome, MNGIE Type +   
Mitochondrial DNA Depletion Syndrome, Myopathic Form +   
Sengers syndrome  

Synonyms
Exact Synonyms: MEPOP ;   MNGIE ;   MNGIE phenotype ;   MNGIE syndrome ;   POLIP ;   POLIP syndrome ;   mitochondrial neurogastrointestinal encephalopathy ;   myoneurogastrointestinal encephalopathy syndrome ;   polyneuropathy, ophthalmoplegia, leukoencephalopathy, and intestinal pseudoobstruction

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