Showing entry for MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 32


　 　 　 　 　 　 　 　 　 　 　 　 　 　 　 　
General Disease Information
BXGD IdBXGD024033
Disease NameMITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 32
Disease CUI IdC4748839
MeSH Codes   
Disease Class Name
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations