Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

Ontology Browser

Term:
Leigh Necrotizing Encephalopathy due to Pyruvate Carboxylase Deficiency (DOID:9004939)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
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  
Subacute Necrotizing Encephalomyelopathy of Leigh, Adult 
Subacute Necrotizing Encephalopathy of Leigh, Infantile  

Synonyms
Exact Synonyms: Leigh syndrome due to pyruvate carboxylase deficiency
Primary IDs: MESH:C536255 ;   RDO:0001757

paths to the root