adisease

Showing entry for Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD019398
Disease Name	Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Disease CUI Id	C3711645
MeSH Codes	C16 C18 C05 C10 C14
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id	HP:0001939 HP:0025354
Human Phenotype Ontology Term	Abnormality of metabolism/homeostasis; Abnormal cellular phenotype
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
P06858	BXGT006515	Lipoprotein lipase	4023	reviewed	Enzyme
P07438	BXGT006625	Metallothionein-1B	4490	reviewed
P55157	BXGT011108	Microsomal triglyceride transfer protein large subunit	4547	reviewed	Transporter
P60484	BXGT011307	Phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN	5728	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}