Showing entry for Congenital hypoplasia of breast



                               
General Disease Information
BXGD IdBXGD005606
Disease NameCongenital hypoplasia of breast
Disease CUI IdC0266013
MeSH Codes C16  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities
Semantic TypeCongenital Abnormality
Human Phenotype Ontology Id HP:0000769  
Human Phenotype Ontology TermAbnormality of the breast
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
O15119 BXGT004128 T-box transcription factor TBX3 6926 reviewed Transcription factor
O43929 BXGT004638 Origin recognition complex subunit 4 5000 reviewed Nucleic acid binding
P01148 BXGT005739 Progonadoliberin-1 2796 reviewed
P03372 BXGT006059 Estrogen receptor 2099 reviewed Nuclear receptor
P11362 BXGT007693 Fibroblast growth factor receptor 1 2260 reviewed Kinase
Q13415 BXGT013350 Origin recognition complex subunit 1 4998 reviewed Nucleic acid binding
Q16828 BXGT013676 Dual specificity protein phosphatase 6 1848 reviewed
Q9H6X2 BXGT020486 Anthrax toxin receptor 1 84168 reviewed Receptor
Q9UHF0 BXGT021699 Tachykinin-3 6866 reviewed
Q9Y6K9 BXGT022333 NF-kappa-B essential modulator 8517 reviewed Kinase
P43146 BXGT022852 Netrin receptor DCC 1630 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