Showing entry for WOLFRAM SYNDROME 2



                               
General Disease Information
BXGD IdBXGD015761
Disease NameWOLFRAM SYNDROME 2
Disease CUI IdC1858028
MeSH Codes C23   C18   C11   C10   C09  
Disease Class NamePathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:630   DOID:225  
Disease Ontology Class Namegenetic disease; syndrome
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
P17655 BXGT008325 Calpain-2 catalytic subunit 824 reviewed Enzyme
Q86WV6 BXGT017626 Stimulator of interferon genes protein 340061 reviewed
Q9NZ45 BXGT021269 CDGSH iron-sulfur domain-containing protein 1 55847 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