DisGeNET - a database of gene-disease associations

diseases

genes

variants

Examples: C0001080, Alzheimer's Disease, D009765, 213200

Hold "" key for selecting multiple diseases

Name:: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2
UMLS CUI:: C1859298
Type:: disease
MeSH Class:: Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
MeSH:: C565865
OMIM:: 213200
Semantic Type:: Disease or Syndrome
Phenotypic abnormality:: None
Disease Ontology:: genetic disease; disease of anatomical entity

Summary of Gene-Disease Associations

Disease Mappings