Showing entry for Immunodeficiency syndrome, variable



                               
General Disease Information
BXGD IdBXGD008232
Disease NameImmunodeficiency syndrome, variable
Disease CUI IdC0398788
MeSH Codes C16   C20  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:630  
Disease Ontology Class Namegenetic disease
Disorder Network disorder-protein-compound-food associations