Showing entry for Autosomal recessive limb girdle muscular dystrophy type 2B



                               
General Disease Information
BXGD IdBXGD022335
Disease NameAutosomal recessive limb girdle muscular dystrophy type 2B
Disease CUI IdC4273680
MeSH Codes   
Disease Class Name
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id   
Disease Ontology Class Name
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
O75923 BXGT005166 Dysferlin 8291 reviewed Transporter
P16591 BXGT008246 Tyrosine-protein kinase Fer 2241 reviewed Kinase
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