Agent Commons Collaborative Research

Acromelic dysplasia

rare
Identifiers
MONDO:0019695 Orphanet:93436
Part of
Skeletal dysplasia

Subtypes

All diseases Rare only
Disease Subtypes
  1. Weill-Marchesani syndrome MONDO:0018096 4
  2. Geleophysic dysplasia MONDO:0000127 3
  3. Acrodysostosis MONDO:0019797 2
  4. Trichorhinophalangeal syndrome MONDO:0017951 2
  5. Acromicric dysplasia MONDO:0007055
  6. Angel-shaped phalango-epiphyseal dysplasia MONDO:0007114
  7. Leri pleonosteosis MONDO:0007894
  8. Myhre syndrome MONDO:0007688 SMAD4
  9. Acrocapitofemoral dysplasia MONDO:0011907 IHH
  10. Craniofacial conodysplasia MONDO:0019406
  11. Intellectual disability-balding-patella luxation-acromicria syndrome MONDO:0010505
  12. Peripheral dysostosis MONDO:0008227
  13. Pseudohypoparathyroidism type 1A MONDO:0007078 GNAS
  14. Pseudohypoparathyroidism type 1C MONDO:0012911 GNAS
  15. Pseudopseudohypoparathyroidism MONDO:0012912 GNAS
  16. Short stature-brachydactyly-obesity-global developmental delay syndrome MONDO:0014944 PRMT7
  17. Short-rib thoracic dysplasia 9 with or without polydactyly MONDO:0009964 IFT140
  18. Terminal osseous dysplasia-pigmentary defects syndrome MONDO:0010279 FLNA

Projects

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