Showing entry for Hemoglobin SC Disease



                               
General Disease Information
BXGD IdBXGD001268
Disease NameHemoglobin SC Disease
Disease CUI IdC0019034
MeSH Codes C16   C15  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:630   DOID:7  
Disease Ontology Class Namegenetic disease; disease of anatomical entity
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
P02549 BXGT005890 Spectrin alpha chain, erythrocytic 1 6708 reviewed
P07204 BXGT006567 Thrombomodulin 7056 reviewed
P09601 BXGT006909 Heme oxygenase 1 3162 reviewed
P19320 BXGT008470 Vascular cell adhesion protein 1 7412 reviewed
P42898 BXGT010344 Methylenetetrahydrofolate reductase 4524 reviewed
P68871 BXGT011615 Hemoglobin subunit beta 3043 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