Acromelic dysplasia

Part of

Sub-types of Acromelic dysplasia

• Pseudohypoparathyroidism type 1A 7 trials
• Pseudopseudohypoparathyroidism 2 trials
• Trichorhinophalangeal syndrome 0 trials · 1 incl. sub-types
  2 sub-types

  • Trichorhinophalangeal syndrome type II 1 trial
  • Trichorhinophalangeal syndrome type I 0 trials
• Acromicric dysplasia 0 trials
• Angel-shaped phalango-epiphyseal dysplasia 0 trials
• Leri pleonosteosis 0 trials
• Myhre syndrome 0 trials
• Weill-Marchesani syndrome 0 trials
  4 sub-types

  • Weill-Marchesani 4 syndrome, recessive 0 trials
  • Weill-Marchesani syndrome 1 0 trials
  • Weill-Marchesani syndrome 2, dominant 0 trials
  • Weill-Marchesani syndrome 3 0 trials
• Acrocapitofemoral dysplasia 0 trials
• Acrodysostosis 0 trials
  2 sub-types

  • Acrodysostosis 1 with or without hormone resistance 0 trials
  • Acrodysostosis 2 with or without hormone resistance 0 trials
• Craniofacial conodysplasia 0 trials
• Geleophysic dysplasia 0 trials
  3 sub-types

  • Geleophysic dysplasia 1 0 trials
  • Geleophysic dysplasia 2 0 trials
  • Geleophysic dysplasia 3 0 trials
• Intellectual disability-balding-patella luxation-acromicria syndrome 0 trials
• Peripheral dysostosis 0 trials
• Pseudohypoparathyroidism type 1C 0 trials
• Short stature-brachydactyly-obesity-global developmental delay syndrome 0 trials
• Short-rib thoracic dysplasia 9 with or without polydactyly 0 trials
• Terminal osseous dysplasia-pigmentary defects syndrome 0 trials