Showing entry for Anemia, hereditary spherocytic hemolytic

General Disease Information
BXGD Id	BXGD004460
Disease Name	Anemia, hereditary spherocytic hemolytic
Disease CUI Id	C0221409
MeSH Codes	C23   C16   C15
Disease Class Name	Pathological Conditions, Signs and Symptoms; 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	DOID:7
Disease Ontology Class Name	disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations