Search for a classification

return to list of classifications

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
        
        Fatty acid hydroxylase-associated neurodegeneration ORPHA:329308

Rare genetic disease ORPHA:98053
- Rare inborn errors of metabolism ORPHA:68367
  - Disorder of lipid metabolism ORPHA:309005
    - Disorder of phospholipids, sphingolipids and fatty acids biosynthesis ORPHA:352301
      - Disorder of phospholipids, sphingolipids and fatty acids biosynthesis with central nervous system predominant involvement ORPHA:352306
        
        Fatty acid hydroxylase-associated neurodegeneration ORPHA:329308

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Genetic neurodegenerative disease ORPHA:183500
    - Hereditary spastic paraplegia ORPHA:685
      - Complex hereditary spastic paraplegia ORPHA:102013
        
        Autosomal recessive complex spastic paraplegia ORPHA:100981
        
        Fatty acid hydroxylase-associated neurodegeneration ORPHA:329308

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Rare genetic movement disorder ORPHA:183521
    - Miscellaneous movement disorder due to genetic neurodegenerative disease ORPHA:307058
      - Neurodegeneration with brain iron accumulation ORPHA:385
        
        Fatty acid hydroxylase-associated neurodegeneration ORPHA:329308

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Genetic neurodegenerative disease ORPHA:183500
    - Genetic neurodegenerative disease with dementia ORPHA:276058
      - Neurodegeneration with brain iron accumulation ORPHA:385
        
        Fatty acid hydroxylase-associated neurodegeneration ORPHA:329308

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Genetic dementia ORPHA:158124
    - Genetic neurodegenerative disease with dementia ORPHA:276058
      - Neurodegeneration with brain iron accumulation ORPHA:385
        
        Fatty acid hydroxylase-associated neurodegeneration ORPHA:329308

Rare genetic disease ORPHA:98053
- Rare genetic neurological disorder ORPHA:71859
  - Neurometabolic disease ORPHA:68385
    - Neurodegeneration with brain iron accumulation ORPHA:385
      - Fatty acid hydroxylase-associated neurodegeneration ORPHA:329308

return to list of classifications

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.