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
The  disease-related  target proteins
Proteins
Uniport Id BXGT Id Protein Name Gene Status Protein Class
Uniport Id BXGT Id Protein name Gene Status Protein class
O00187 BXGT003890 Mannan-binding lectin serine protease 2 10747 reviewed Enzyme
O00602 BXGT003940 Ficolin-1 2219 reviewed Signaling
O75636 BXGT005141 Ficolin-3 8547 reviewed Signaling
P11226 BXGT007675 Mannose-binding protein C 4153 reviewed Receptor
Q15485 BXGT013574 Ficolin-2 2220 reviewed Signaling
The  disease-related  compounds
Compounds
BXGC Id Compound Name Structure Molecular Weight Number of targets?Number of times compound connecting the disease , higher numbers indicate the compound is more associated with the disease
The  disease-related  foods
Foods
BXGF Id Food Name Scientific Name Food Group Number of compounds in food?Number of compounds in food that connecting disease, higher numbers indicate the more compounds in food are more associated with the dusease