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Orphanet classification of rare genetic diseases

Rare genetic disease ORPHA:98053
- Rare inborn errors of metabolism ORPHA:68367
  - Disorder of metabolite absorption and transport ORPHA:309824
    - Disorder of mineral absorption and transport ORPHA:309836
      - Disorder of iron metabolism and transport ORPHA:309842
        
        Congenital atransferrinemia ORPHA:1195

Rare genetic disease ORPHA:98053
- Rare genetic hematologic disease ORPHA:158300
  - Rare constitutional anemia ORPHA:183651
    - Constitutional deficiency anemia ORPHA:248296
      - Constitutional anemia due to iron metabolism disorder ORPHA:98360
        
        Congenital atransferrinemia ORPHA:1195

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