Showing entry for Trisomy 21, Mitotic Nondisjunction



                               
General Disease Information
BXGD IdBXGD010315
Disease NameTrisomy 21, Mitotic Nondisjunction
Disease CUI IdC0751081
MeSH Codes C16   C10  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous 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
P00441 BXGT005540 Superoxide dismutase [Cu-Zn] 6647 reviewed Enzyme
P04271 BXGT006177 Protein S100-B 6285 reviewed Calcium-binding protein
P10145 BXGT007542 Interleukin-8 3576 reviewed Signaling
P28161 BXGT009234 Glutathione S-transferase Mu 2 2946 reviewed
P30041 BXGT009393 Peroxiredoxin-6 9588 reviewed Enzyme
P32119 BXGT009600 Peroxiredoxin-2 7001 reviewed Enzyme
P41440 BXGT010261 Folate transporter 1 6573 reviewed Transporter
P42898 BXGT010344 Methylenetetrahydrofolate reductase 4524 reviewed
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