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Ontology Browser

Term:
Leigh Syndrome due to Mitochondrial Complex III Deficiency (DOID:9000679)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
Leigh disease +     
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome  
CoQ-Responsive OXPHOS Deficiency 
French Canadian Leigh disease  
Leigh Necrotizing Encephalopathy due to Pyruvate Carboxylase Deficiency 
Leigh Syndrome Due To Mitochondrial Complex I Deficiency  
Leigh Syndrome due to Mitochondrial Complex II Deficiency  
Leigh Syndrome due to Mitochondrial Complex III Deficiency  
Leigh Syndrome due to Mitochondrial Complex IV Deficiency  
Leigh Syndrome due to Mitochondrial Complex V Deficiency 
Leigh Syndrome, X-Linked  
Lipoyltransferase 1 Deficiency  
Maternally Inherited Leigh Syndrome  
MITOCHONDRIAL SHORT-CHAIN ENOYL-COA HYDRATASE 1 DEFICIENCY  
Necrotizing Encephalomyelopathy, Subacute, of Leigh, Adult 
Necrotizing Encephalopathy, Infantile Subacute, of Leigh 

Synonyms
Primary IDs: MESH:C564962 ;   RDO:0013742

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