Showing entry for Neurogenic Muscular Atrophy



                               
General Disease Information
BXGD IdBXGD006137
Disease NameNeurogenic Muscular Atrophy
Disease CUI IdC0270948
MeSH Codes C23   C10  
Disease Class NamePathological Conditions, Signs and Symptoms; Nervous System Diseases
Semantic TypePathologic Function
Human Phenotype Ontology Id HP:0003011  
Human Phenotype Ontology TermAbnormality of the musculature
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations