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Orphanet classification of rare developmental anomalies during embryogenesis

Rare developmental defect during embryogenesis ORPHA:93890
- Rare developmental defect with connective tissue involvement ORPHA:139030
  - Blindness-scoliosis-arachnodactyly syndrome ORPHA:171844
  - Connective tissue disorder due to lysyl hydroxylase-3 deficiency ORPHA:300284
  - Cutis laxa ORPHA:209
  - Cutis laxa-Marfanoid syndrome ORPHA:171719
  - Desbuquois syndrome ORPHA:1425
  - Ehlers-Danlos/osteogenesis imperfecta syndrome ORPHA:230857
  - Ehlers-Danlos syndrome ORPHA:98249
  - Familial articular hypermobility syndrome ORPHA:2295
  - Grange syndrome ORPHA:79094
  - Larsen-like syndrome, B3GAT3 type ORPHA:284139
  - Larsen syndrome ORPHA:503
  - Lethal Larsen-like syndrome ORPHA:2371
  - Marfanoid habitus-inguinal hernia-advanced bone age syndrome ORPHA:314041
  - Marfan syndrome ORPHA:558
  - Polyvalvular heart disease syndrome ORPHA:228410
  - Pseudodiastrophic dysplasia ORPHA:85174
  - Pseudoxanthoma elasticum ORPHA:758
  - Severe myopia-generalized joint laxity-short stature syndrome ORPHA:527450

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