Showing entry for Pure hereditary spastic paraplegia

General Disease Information
BXGD Id	BXGD008088
Disease Name	Pure hereditary spastic paraplegia
Disease CUI Id	C0393555
MeSH Codes	C16   C10
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations