Showing entry for Scleroderma, Limited



                               
General Disease Information
BXGD IdBXGD010199
Disease NameScleroderma, Limited
Disease CUI IdC0748540
MeSH Codes C17  
Disease Class NameSkin and Connective Tissue 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
P01911 BXGT005816 HLA class II histocompatibility antigen, DRB1-15 beta chain 3123 reviewed Immune response
P20273 BXGT008557 B-cell receptor CD22 933 reviewed
P35555 BXGT009845 Fibrillin-1 2200 reviewed Calcium-binding protein
P51684 BXGT010880 C-C chemokine receptor type 6 1235 reviewed G-protein coupled receptor
Q15063 BXGT013531 Periostin 10631 reviewed Signaling
Q8IZA0 BXGT025026 Dyslexia-associated protein KIAA0319-like protein 79932 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