Showing entry for Hereditary persistence of fetal hemoglobin thalassemia

General Disease Information
BXGD Id	BXGD006290
Disease Name	Hereditary persistence of fetal hemoglobin thalassemia
Disease CUI Id	C0271994
MeSH Codes	C16   C15
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations