Showing entry for Congenital absence of adrenal gland



                               
General Disease Information
BXGD IdBXGD005640
Disease NameCongenital absence of adrenal gland
Disease CUI IdC0266273
MeSH Codes C16   C20   C19  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Endocrine System Diseases
Semantic TypeCongenital Abnormality
Human Phenotype Ontology Id HP:0000818  
Human Phenotype Ontology TermAbnormality of the endocrine system
Disease Ontology Id DOID:7  
Disease Ontology Class Namedisease 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
P56703 BXGT023722 Proto-oncogene Wnt-3 7473 reviewed Signaling
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