Showing entry for Congenital hypogonadotropic hypogonadism



                               
General Disease Information
BXGD IdBXGD020084
Disease NameCongenital hypogonadotropic hypogonadism
Disease CUI IdC3899503
MeSH Codes C16   C19  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System 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
O95631 BXGT005387 Netrin-1 9423 reviewed Enzyme modulator
P01148 BXGT005739 Progonadoliberin-1 2796 reviewed
P01215 BXGT005743 Glycoprotein hormones alpha chain 1081 reviewed
P11362 BXGT007693 Fibroblast growth factor receptor 1 2260 reviewed Kinase
Q86Z14 BXGT017639 Beta-klotho 152831 reviewed Enzyme
Q9UHF0 BXGT021699 Tachykinin-3 6866 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