MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, UMDF: 1= Disease, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, Myopathy, SANDO
Term ID:6879
Name:Leigh Syndrome due to Mitochondrial Complex V Deficiency
Definition:
Alternative IDs:
ParentIDs:MESH:D007888
TreeNumbers:C10.228.140.163.100.412/C564964 |C16.320.565.189.412/C564964 |C16.320.565.202.810.444/C564964 |C18.452.132.100.412/C564964 |C18.452.648.189.412/C564964 |C18.452.648.202.810.444/C564964 |C18.452.660.520/C564964
Synonyms:
Slim Mappings:Genetic disease (inborn)|Metabolic disease|Nervous system disease
Reference: MedGen: C564964
MeSH: C564964
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal