Showing entry for Dentinogenesis imperfecta without osteogenesis imperfecta



                               
General Disease Information
BXGD IdBXGD018203
Disease NameDentinogenesis imperfecta without osteogenesis imperfecta
Disease CUI IdC2973527
MeSH Codes C16   C07  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic 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
O95551 BXGT005384 Tyrosyl-DNA phosphodiesterase 2 51567 reviewed
P52895 BXGT010961 Aldo-keto reductase family 1 member C2 1646 reviewed Enzyme
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