8p23.1 microdeletion syndrome

From BugSigDB

8p23.1 deletion involves a partial deletion of the short arm of chromosome 8 characterized by low birth weight, postnatal growth deficiency, mild intellectual deficit, hyperactivity, craniofacial abnormalities, and congenital heart defects.
  • 8p23.1 deletion
  • 8p23.1 microdeletion syndrome
  • chromosome 8p23.1 deletion
  • Del(8)(p23.1)
  • deletion 8p23.1
  • Monosomy 8p23.1
  • monosomy 8p23.1