Showing entry for Aplasia/Hypoplasia of the mandible



                               
General Disease Information
BXGD IdBXGD021330
Disease NameAplasia/Hypoplasia of the mandible
Disease CUI IdC4024589
MeSH Codes   
Disease Class Name
Semantic TypeAnatomical Abnormality
Human Phenotype Ontology Id HP:0000152   HP:0000924  
Human Phenotype Ontology TermAbnormality of head or neck; Abnormality of the skeletal system
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
O95166 BXGT005353 Gamma-aminobutyric acid receptor-associated protein 11337 reviewed Cellular structure
P02545 BXGT005889 Prelamin-A/C 4000 reviewed
P22607 BXGT008784 Fibroblast growth factor receptor 3 2261 reviewed Kinase
P24385 BXGT008965 G1/S-specific cyclin-D1 595 reviewed Enzyme modulator
P78352 BXGT011836 Disks large homolog 4 1742 reviewed Receptor
Q13635 BXGT024910 Protein patched homolog 1 5727 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