Showing entry for Anemia, Hemolytic, Congenital Nonspherocytic

General Disease Information
BXGD Id	BXGD000141
Disease Name	Anemia, Hemolytic, Congenital Nonspherocytic
Disease CUI Id	C0002882
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	DOID:7
Disease Ontology Class Name	disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations