Showing entry for Hemoglobin D trait



                               
General Disease Information
BXGD IdBXGD006301
Disease NameHemoglobin D trait
Disease CUI IdC0272081
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