adisease

Showing entry for Deficiency of acetyl-CoA acetyltransferase

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD013345
Disease Name	Deficiency of acetyl-CoA acetyltransferase
Disease CUI Id	C1536500
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	DOID:630
Disease Ontology Class Name	genetic disease
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
P0DN79	BXGT007511	Cystathionine beta-synthase-like protein	875	reviewed
P24752	BXGT008993	Acetyl-CoA acetyltransferase, mitochondrial	38	reviewed	Enzyme
P35520	BXGT009842	Cystathionine beta-synthase	875	reviewed
P55809	BXGT011127	Succinyl-CoA:3-ketoacid coenzyme A transferase 1, mitochondrial	5019	reviewed	Enzyme
Q9BWD1	BXGT020152	Acetyl-CoA acetyltransferase, cytosolic	39	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}