Showing entry for Dysfibrinogenemia, Congenital

General Disease Information
BXGD Id	BXGD006354
Disease Name	Dysfibrinogenemia, Congenital
Disease CUI Id	C0272350
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