Showing entry for Thyroid Agenesis



                               
General Disease Information
BXGD IdBXGD010216
Disease NameThyroid Agenesis
Disease CUI IdC0749420
MeSH Codes C16   C19  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases
Semantic TypeCongenital Abnormality
Human Phenotype Ontology Id HP:0000818  
Human Phenotype Ontology TermAbnormality of the endocrine system
Disease Ontology Id DOID:630   DOID:7  
Disease Ontology Class Namegenetic disease; disease 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
P16473 BXGT008234 Thyrotropin receptor 7253 reviewed G-protein coupled receptor
P52952 BXGT010966 Homeobox protein Nkx-2.5 1482 reviewed Transcription factor
Q06710 BXGT012887 Paired box protein Pax-8 7849 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