Showing entry for Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia



                               
General Disease Information
BXGD IdBXGD015308
Disease NameDeafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia
Disease CUI IdC1853144
MeSH Codes C23   C16   C10   C07   C09  
Disease Class NamePathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
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
P15328 BXGT008108 Folate receptor alpha 2348 reviewed
P21589 BXGT008669 5'-nucleotidase 4907 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