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Diseases

Genetic and Rare Diseases Information Center (GARD)

Chromosome 17q11.2 deletion syndrome


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Other Names for Chromosome 17q11.2 deletion syndrome

  • 17q11 microdeletion syndrome
  • Chromosome 17q11.2 deletion syndrome, 1.4Mb
  • Del(17)(q11)
  • Maternal uniparental disomy of chromosome 13
  • Monosomy 17q11
  • Neurofibromatosis type 1 microdeletion syndrome
  • NF1 microdeletion syndrome
  • Paternal uniparental disomy 13
  • Uniparental disomy of chromosome 13
  • UPD(13)
  • VAN ASPEREN SYNDROME
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.