Showing entry for Proopiomelanocortin Deficiency



                               
General Disease Information
BXGD IdBXGD015755
Disease NameProopiomelanocortin Deficiency
Disease CUI IdC1857854
MeSH Codes C23   C18   C19  
Disease Class NamePathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Endocrine System 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
P01189 BXGT005742 Pro-opiomelanocortin 5443 reviewed
P32245 BXGT009614 Melanocortin receptor 4 4160 reviewed G-protein coupled receptor
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