adisease

Showing entry for HMG CoA lyase deficiency

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD006002
Disease Name	HMG CoA lyase deficiency
Disease CUI Id	C0268601
MeSH Codes	C16 C18
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations

The disease-related target proteins

Proteins

Uniport Id	BXGT Id	Protein Name	Gene	Status	Protein Class
Uniport Id	BXGT Id	Protein name	Gene	Status	Protein class
P00480	BXGT005551	Ornithine carbamoyltransferase, mitochondrial	5009	reviewed
P01130	BXGT005735	Low-density lipoprotein receptor	3949	reviewed
P11597	BXGT007727	Cholesteryl ester transfer protein	1071	reviewed
P35914	BXGT009880	Hydroxymethylglutaryl-CoA lyase, mitochondrial	3155	reviewed	Enzyme

The disease-related compounds

Compounds

BXGC Id	Compound Name	Structure	Molecular Weight	Number of targets^{?Number of times compound connecting the disease , higher numbers indicate the compound is more associated with the disease}

The disease-related foods

Foods

BXGF Id	Food Name	Scientific Name	Food Group	Number of compounds in food^{?Number of compounds in food that connecting disease, higher numbers indicate the more compounds in food are more associated with the dusease}