Showing entry for Impaired memory B cell generation

General Disease Information
BXGD Id	BXGD021723
Disease Name	Impaired memory B cell generation
Disease CUI Id	C4025672
MeSH Codes
Disease Class Name
Semantic Type	Cell or Molecular Dysfunction
Human Phenotype Ontology Id	HP:0001939   HP:0002715   HP:0025354
Human Phenotype Ontology Term	Abnormality of metabolism/homeostasis; Abnormality of the immune system; Abnormal cellular phenotype
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations