Details of Disease

General Information of Disease (ID: DISQGHO3)

• Disease Name: Autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome
• Disease Hierarchy:
  DISWBOUC: Autosomal recessive cerebellar ataxia
  DIS80GDF: Monogenic epilepsy
  DISQGHO3: Autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome
• Disease Identifiers:
  MONDO ID: MONDO_0018446
  UMLS CUI: C5681145
  MedGen ID: 1843349
  Orphanet ID: 404481