Showing entry for MASP2 Deficiency



                               
General Disease Information
BXGD IdBXGD018392
Disease NameMASP2 Deficiency
Disease CUI IdC3151085
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   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations