Showing entry for Craniodiaphyseal dysplasia



                               
General Disease Information
BXGD IdBXGD008435
Disease NameCraniodiaphyseal dysplasia
Disease CUI IdC0410539
MeSH Codes C16   C05  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Semantic TypeDisease or Syndrome
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
O76039 BXGT005171 Cyclin-dependent kinase-like 5 6792 reviewed Kinase
P10145 BXGT007542 Interleukin-8 3576 reviewed Signaling
P32320 BXGT009622 Cytidine deaminase 978 reviewed Enzyme
P42262 BXGT010294 Glutamate receptor 2 2891 reviewed Ion channel
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