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Orphanet classification of rare developmental anomalies during embryogenesis

Rare developmental defect during embryogenesis ORPHA:93890
- Rare bone development disorder ORPHA:139012
  - Primary bone dysplasia ORPHA:364526
    - Primary bone dysplasia with defective bone mineralization ORPHA:93447
      - Disorders of vitamin D metabolism ORPHA:289098
      - Eiken syndrome ORPHA:79106
      - Familial calcium pyrophosphate deposition ORPHA:1416
      - Familial hypocalciuric hypercalcemia ORPHA:405
      - Hypophosphatasia ORPHA:436
      - Lipodystrophy-intellectual disability-deafness syndrome ORPHA:50811
      - Neonatal severe primary hyperparathyroidism ORPHA:417
      - Oculoskeletodental syndrome ORPHA:557003
      - Ossification anomalies-psychomotor developmental delay syndrome ORPHA:73230

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