Showing entry for MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1C



                               
General Disease Information
BXGD IdBXGD013853
Disease NameMUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1C
Disease CUI IdC1832567
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
O75923 BXGT005166 Dysferlin 8291 reviewed Transporter
P04083 BXGT006147 Annexin A1 301 reviewed
O14793 BXGT023280 Growth/differentiation factor 8 2660 reviewed Signaling
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