Showing entry for Glycogen Storage Disease Type VII



                               
General Disease Information
BXGD IdBXGD001157
Disease NameGlycogen Storage Disease Type VII
Disease CUI IdC0017926
MeSH Codes C16   C18   C05   C10  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:0014667   DOID:630  
Disease Ontology Class Namedisease of metabolism; 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
P07741 BXGT006666 Adenine phosphoribosyltransferase 353 reviewed
P11217 BXGT007674 Glycogen phosphorylase, muscle form 5837 reviewed Enzyme
P29218 BXGT009322 Inositol monophosphatase 1 3612 reviewed Enzyme
P35557 BXGT009846 Glucokinase 2645 reviewed Kinase
Q16665 BXGT013653 Hypoxia-inducible factor 1-alpha 3091 reviewed Transcription factor
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