Showing entry for Congenital neutropenia, myelofibrosis, nephromegaly syndrome

General Disease Information
BXGD Id	BXGD024086
Disease Name	Congenital neutropenia, myelofibrosis, nephromegaly syndrome
Disease CUI Id	C4755251
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