Showing entry for Porencephaly



                               
General Disease Information
BXGD IdBXGD022087
Disease NamePorencephaly
Disease CUI IdC4082173
MeSH Codes C16   C05   C10  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System 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
P02462 BXGT005881 Collagen alpha-1(IV) chain 1282 reviewed
P08572 BXGT006791 Collagen alpha-2(IV) chain 1284 reviewed
P10275 BXGT007552 Androgen receptor 367 reviewed Nuclear receptor
Q71U36 BXGT016705 Tubulin alpha-1A chain 7846 reviewed Cellular structure
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