Showing entry for Acid cholesteryl ester hydrolase deficiency, type 2



                               
General Disease Information
BXGD IdBXGD018139
Disease NameAcid cholesteryl ester hydrolase deficiency, type 2
Disease CUI IdC2936797
MeSH Codes C16   C18  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
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
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
O75908 BXGT005162 Sterol O-acyltransferase 2 8435 reviewed Enzyme
P24298 BXGT008960 Alanine aminotransferase 1 2875 reviewed Enzyme
P38571 BXGT010054 Lysosomal acid lipase/cholesteryl ester hydrolase 3988 reviewed Enzyme
P51149 BXGT010835 Ras-related protein Rab-7a 7879 reviewed
P55774 BXGT011124 C-C motif chemokine 18 6362 reviewed Signaling
Q13231 BXGT013329 Chitotriosidase-1 1118 reviewed
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