Showing entry for Complement component 5 deficiency



                               
General Disease Information
BXGD IdBXGD007591
Disease NameComplement component 5 deficiency
Disease CUI IdC0343047
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:7  
Disease Ontology Class Namedisease of anatomical entity
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
P00450 BXGT005544 Ceruloplasmin 1356 reviewed Enzyme
P01031 BXGT005720 Complement C5 727 reviewed Enzyme modulator
P06213 BXGT006425 Insulin receptor 3643 reviewed Kinase
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