Showing entry for Neutropenia, Severe Congenital, X-Linked

General Disease Information
BXGD Id	BXGD014770
Disease Name	Neutropenia, Severe Congenital, X-Linked
Disease CUI Id	C1845987
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
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations