Showing entry for Hereditary liability to pressure palsies



                               
General Disease Information
BXGD IdBXGD008149
Disease NameHereditary liability to pressure palsies
Disease CUI IdC0393814
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: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
P08034 BXGT006716 Gap junction beta-1 protein 2705 reviewed Cell-cell junction
P10275 BXGT007552 Androgen receptor 367 reviewed Nuclear receptor
P16278 BXGT008213 Beta-galactosidase 2720 reviewed Enzyme
P60903 BXGT011339 Protein S100-A10 6281 reviewed Calcium-binding protein
Q01453 BXGT012588 Peripheral myelin protein 22 5376 reviewed Cellular structure
Q9Y6Y9 BXGT022346 Lymphocyte antigen 96 23643 reviewed Receptor
O43148 BXGT023017 mRNA cap guanine-N7 methyltransferase 8731 reviewed
O95140 BXGT024482 Mitofusin-2 9927 reviewed Enzyme
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