Showing entry for Developmental absence of tooth



                               
General Disease Information
BXGD IdBXGD008236
Disease NameDevelopmental absence of tooth
Disease CUI IdC0399352
MeSH Codes C16   C07  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
Semantic TypeCongenital Abnormality
Human Phenotype Ontology Id HP:0000152  
Human Phenotype Ontology TermAbnormality of head or neck
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
P01375 BXGT005753 Tumor necrosis factor 7124 reviewed Signaling
P11226 BXGT007675 Mannose-binding protein C 4153 reviewed Receptor
P11362 BXGT007693 Fibroblast growth factor receptor 1 2260 reviewed Kinase
P21333 BXGT008638 Filamin-A 2316 reviewed
P27482 BXGT009185 Calmodulin-like protein 3 810 reviewed Calcium-binding protein
P51812 BXGT010893 Ribosomal protein S6 kinase alpha-3 6197 reviewed Kinase
Q13698 BXGT013392 Voltage-dependent L-type calcium channel subunit alpha-1S 779 reviewed Ion channel
Q14332 BXGT013462 Frizzled-2 2535 reviewed G-protein coupled receptor
Q14623 BXGT013490 Indian hedgehog protein 3549 reviewed
Q15223 BXGT013551 Nectin-1 5818 reviewed
Q16539 BXGT013634 Mitogen-activated protein kinase 14 1432 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