Showing entry for ERYTHROCYTOSIS, FAMILIAL, 2

General Disease Information
BXGD Id	BXGD014286
Disease Name	ERYTHROCYTOSIS, FAMILIAL, 2
Disease CUI Id	C1837915
MeSH Codes	C15
Disease Class Name	Hemic and Lymphatic Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630   DOID:7
Disease Ontology Class Name	genetic disease; disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations