Showing entry for Myotubular (centronuclear) myopathy



                               
General Disease Information
BXGD IdBXGD017838
Disease NameMyotubular (centronuclear) myopathy
Disease CUI IdC2875316
MeSH Codes   
Disease Class Name
Semantic TypeCongenital 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