Showing entry for Complicated hereditary spastic paraplegia



                               
General Disease Information
BXGD IdBXGD008089
Disease NameComplicated hereditary spastic paraplegia
Disease CUI IdC0393556
MeSH Codes C16   C10  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations