19p13.12 microdeletion syndrome

From BugSigDB


19p13.12 microdeletion syndrome is a newly described syndrome characterized by moderate to severe developmental delay, language delay, bilateral sensorineural and/or conductive hearing loss and facial dysmorphism.
Aliases
  • 19p13.12 microdeletion syndrome
  • Chromosome19p13.12 microdeletion
  • Del(19)(p13.12)
  • Monosomy 19p13.12
  • monosomy 19p13.12