Showing entry for Osteogenesis imperfecta type IV (disorder)



                               
General Disease Information
BXGD IdBXGD005916
Disease NameOsteogenesis imperfecta type IV (disorder)
Disease CUI IdC0268363
MeSH Codes   
Disease Class Name
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
P02452 BXGT005878 Collagen alpha-1(I) chain 1277 reviewed
P09486 BXGT006897 SPARC 6678 reviewed Signaling
P23284 BXGT008845 Peptidyl-prolyl cis-trans isomerase B 5479 reviewed
P36955 BXGT009946 Pigment epithelium-derived factor 5176 reviewed Enzyme modulator
P08123 BXGT024477 Collagen alpha-2(I) chain 1278 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