Showing entry for Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder)



                               
General Disease Information
BXGD IdBXGD008409
Disease NameSevere autosomal recessive muscular dystrophy of childhood - North African type (disorder)
Disease CUI IdC0410173
MeSH Codes C16   C05   C08   C10   C14  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Respiratory Tract Diseases; Nervous System Diseases; Cardiovascular 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