Showing entry for Congenital, Hereditary, and Neonatal Diseases and Abnormalities

General Disease Information
BXGD Id	BXGD002003
Disease Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Disease CUI Id	C0027612
MeSH Codes	C16
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Semantic Type	Disease or Syndrome; Congenital Abnormality
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations