Showing entry for COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 13

General Disease Information
BXGD Id	BXGD019201
Disease Name	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 13
Disease CUI Id	C3554129
MeSH Codes
Disease Class Name
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:0014667   DOID:630
Disease Ontology Class Name	disease of metabolism; genetic disease
Disorder Network	disorder-protein-compound-food associations