Showing entry for Spastic paraplegia 13, autosomal dominant

General Disease Information
BXGD Id	BXGD015406
Disease Name	Spastic paraplegia 13, autosomal dominant
Disease CUI Id	C1854467
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	DOID:630   DOID:7
Disease Ontology Class Name	genetic disease; disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations