Showing entry for Congenital Structural Myopathy



                               
General Disease Information
BXGD IdBXGD010709
Disease NameCongenital Structural Myopathy
Disease CUI IdC0752282
MeSH Codes C05   C10  
Disease Class NameMusculoskeletal 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