Showing entry for Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Dominant

General Disease Information
BXGD Id	BXGD017243
Disease Name	Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Dominant
Disease CUI Id	C2674321
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	DOID:630   DOID:7
Disease Ontology Class Name	genetic disease; disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations