Showing entry for Osteodystrophy



                               
General Disease Information
BXGD IdBXGD005361
Disease NameOsteodystrophy
Disease CUI IdC0264009
MeSH Codes C18   C05  
Disease Class NameNutritional and Metabolic Diseases; Musculoskeletal Diseases
Semantic TypeDisease or Syndrome; Congenital Abnormality
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
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
P01270 BXGT005746 Parathyroid hormone 5741 reviewed
P27037 BXGT009153 Activin receptor type-2A 92 reviewed Kinase
P63092 BXGT011495 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short 2778 reviewed
Q9HC97 BXGT020527 G-protein coupled receptor 35 2859 reviewed G-protein coupled receptor
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