Showing entry for Factor XIII, B Subunit, Deficiency Of

General Disease Information
BXGD Id	BXGD017667
Disease Name	Factor XIII, B Subunit, Deficiency Of
Disease CUI Id	C2750481
MeSH Codes	C16   C15
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Semantic Type	Finding
Human Phenotype Ontology Id	HP:0001871
Human Phenotype Ontology Term	Abnormality of blood and blood-forming tissues
Disease Ontology Id	DOID:630   DOID:7
Disease Ontology Class Name	genetic disease; disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations