Showing entry for Factor II mutation

General Disease Information
BXGD Id	BXGD013451
Disease Name	Factor II mutation
Disease CUI Id	C1610621
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