Showing entry for Myopathy, Centronuclear, Autosomal Recessive



                               
General Disease Information
BXGD IdBXGD008418
Disease NameMyopathy, Centronuclear, Autosomal Recessive
Disease CUI IdC0410204
MeSH Codes C05   C10  
Disease Class NameMusculoskeletal Diseases; Nervous System Diseases
Semantic TypeDisease or Syndrome; Congenital Abnormality
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
P21817 BXGT008693 Ryanodine receptor 1 6261 reviewed Ion channel
P49418 BXGT010704 Amphiphysin 273 reviewed
Q8WZ42 BXGT019023 Titin 7273 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