Showing entry for SPINOCEREBELLAR ATAXIA 26



                               
General Disease Information
BXGD IdBXGD014113
Disease NameSPINOCEREBELLAR ATAXIA 26
Disease CUI IdC1836395
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 DOID:630   DOID:7  
Disease Ontology Class Namegenetic disease; disease of anatomical entity
Disorder Network disorder-protein-compound-food associations