Showing entry for Properdin Deficiency, Type III

General Disease Information
BXGD Id	BXGD014377
Disease Name	Properdin Deficiency, Type III
Disease CUI Id	C1839456
MeSH Codes	C16   C20
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System 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