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Orphanet classification of rare genetic diseases

Rare genetic disease ORPHA:98053
- Rare genetic endocrine disease ORPHA:156638
  - Genetic endocrine growth disease ORPHA:156643
    - Non-acquired pituitary hormone deficiency ORPHA:95488
      - Non-acquired isolated growth hormone deficiency ORPHA:631
        
        Isolated growth hormone deficiency type IA ORPHA:231662
        
        Isolated growth hormone deficiency type IB ORPHA:231671
        
        Isolated growth hormone deficiency type II ORPHA:231679
        
        Isolated growth hormone deficiency type III ORPHA:231692
        
        Short stature due to growth hormone qualitative anomaly ORPHA:629

Rare genetic disease ORPHA:98053
- Rare genetic endocrine disease ORPHA:156638
  - Rare genetic hypothalamic or pituitary disease ORPHA:183628
    - Pituitary deficiency ORPHA:101957
      - Non-acquired pituitary hormone deficiency ORPHA:95488
        
        Non-acquired isolated growth hormone deficiency ORPHA:631
        
        Isolated growth hormone deficiency type IA ORPHA:231662
        
        Isolated growth hormone deficiency type IB ORPHA:231671
        
        Isolated growth hormone deficiency type II ORPHA:231679
        
        Isolated growth hormone deficiency type III ORPHA:231692
        
        Short stature due to growth hormone qualitative anomaly ORPHA:629

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