Showing entry for Neutropenia, Severe Congenital, Autosomal Dominant 1

General Disease Information
BXGD Id	BXGD015943
Disease Name	Neutropenia, Severe Congenital, Autosomal Dominant 1
Disease CUI Id	C1859966
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
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations