Showing entry for ELLIPTOCYTOSIS 2 (disorder)

General Disease Information
BXGD Id	BXGD015232
Disease Name	ELLIPTOCYTOSIS 2 (disorder)
Disease CUI Id	C1851741
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