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Orphanet classification of rare genetic diseases

Rare genetic disease ORPHA:98053
- Rare genetic eye disease ORPHA:101435
  - Rare genetic disorder of the visual organs ORPHA:522504
    - Genetic neuro-ophthalmological disease ORPHA:183616
      - Rare genetic ophthalmic disorder with cranial nerve involvement ORPHA:522510
        
        Rare genetic optic nerve disorder ORPHA:522512
        
        Hereditary optic neuropathy ORPHA:98671
        
        Syndromic hereditary optic neuropathy ORPHA:441434
        
        Spastic paraplegia type 7 ORPHA:99013

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Genetic neurodegenerative disease ORPHA:183500
    - Hereditary spastic paraplegia ORPHA:685
      - Pure or complex hereditary spastic paraplegia ORPHA:320335
        
        Pure or complex autosomal recessive spastic paraplegia ORPHA:320346
        
        Spastic paraplegia type 7 ORPHA:99013

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Genetic neurodegenerative disease ORPHA:183500
    - Hereditary spastic paraplegia ORPHA:685
      - Pure or complex hereditary spastic paraplegia ORPHA:320335
        
        Pure or complex autosomal dominant spastic paraplegia ORPHA:320342
        
        Spastic paraplegia type 7 ORPHA:99013

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Rare hereditary ataxia ORPHA:183518
    - Spastic paraplegia type 7 ORPHA:99013

Rare genetic disease ORPHA:98053
- Rare inborn errors of metabolism ORPHA:68367
  - Disorder of energy metabolism ORPHA:79200
    - Mitochondrial disease ORPHA:68380
      - Mitochondrial oxidative phosphorylation disorder ORPHA:223713
        
        Mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies ORPHA:2443
        
        Mitochondrial disorder due to a defect in mitochondrial protein synthesis ORPHA:35696
        
        Spastic paraplegia type 7 ORPHA:99013

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