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Orphanet classification of rare neurological diseases

Rare neurologic disease ORPHA:98006
- Neurometabolic disease ORPHA:68385
  - Congenital disorder of glycosylation with neurological involvement ORPHA:371047
    - Congenital disorder of glycosylation with epilepsy as a major feature ORPHA:371071
      - SSR4-CDG ORPHA:370927

Rare neurologic disease ORPHA:98006
- Rare epilepsy ORPHA:101998
  - Metabolic diseases with epilepsy ORPHA:166481
    - Congenital disorder of glycosylation with epilepsy as a major feature ORPHA:371071
      - SSR4-CDG ORPHA:370927

Rare neurologic disease ORPHA:98006
- Rare intellectual disability ORPHA:87277
  - Rare syndromic intellectual disability ORPHA:102369
    - X-linked syndromic intellectual disability ORPHA:98464
      - SSR4-CDG ORPHA:370927

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