Showing entry for Spinocerebellar ataxia type 38

General Disease Information
BXGD Id	BXGD023018
Disease Name	Spinocerebellar ataxia type 38
Disease CUI Id	C4518337
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