Showing entry for CCHS WITH HIRSCHSPRUNG DISEASE



                               
General Disease Information
BXGD IdBXGD015846
Disease NameCCHS WITH HIRSCHSPRUNG DISEASE
Disease CUI IdC1859049
MeSH Codes C23   C08   C10  
Disease Class NamePathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases
Semantic TypeDisease or Syndrome; Congenital Abnormality
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
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
P07949 BXGT006703 Proto-oncogene tyrosine-protein kinase receptor Ret 5979 reviewed Kinase
P15538 BXGT008137 Cytochrome P450 11B1, mitochondrial 1584 reviewed
P19099 BXGT008456 Cytochrome P450 11B2, mitochondrial 1585 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