Showing entry for beta Thalassemia, heterozygous



                               
General Disease Information
BXGD IdBXGD011366
Disease Namebeta Thalassemia, heterozygous
Disease CUI IdC0878520
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   
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
P02042 BXGT005834 Hemoglobin subunit delta 3045 reviewed
P02786 BXGT005961 Transferrin receptor protein 1 7037 reviewed Enzyme
P68871 BXGT011615 Hemoglobin subunit beta 3043 reviewed
P69905 BXGT011649 Hemoglobin subunit alpha 3040 reviewed
Q8WWM9 BXGT019001 Cytoglobin 114757 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