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Diseases

Genetic and Rare Diseases Information Center (GARD)

Schwartz Jampel syndrome type 1


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Other Names for Schwartz Jampel syndrome type 1

  • SJS1
  • Schwartz Jampel syndrome
  • Schwartz Jampel Aberfeld syndrome
  • Myotonic myopathy dwarfism chondrodystrophy and ocular and facial abnormalities
  • SJA syndrome
  • Chondrodystrophic myotonia
  • Aberfeld syndrome
  • Burton disease
  • Burton skeletal dysplasia
  • Catel-Hempel syndrome
  • Dysostosis enchondralis metaepiphysaria, Catel-Hempel type
  • Myotonic chondrodystrophy
  • Myotonic myopathy, dwarfism, chondrodystrophy, ocular and facial anomalies
  • Osteochondromuscular dystrophy
  • Schwartz-Jampel syndrome
  • Schwartz-Jampel syndrome type 1
  • Schwartz-Jampel-Aberfeld syndrome
  • Burton syndrome
  • SJS
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.