Showing entry for Complement Component 7 Deficiency

General Disease Information
BXGD Id	BXGD016243
Disease Name	Complement Component 7 Deficiency
Disease CUI Id	C1864694
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	DOID:7
Disease Ontology Class Name	disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations