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.
- Aliases
- 8p23.1 deletion
- 8p23.1 microdeletion syndrome
- chromosome 8p23.1 deletion
- Del(8)(p23.1)
- deletion 8p23.1
- Monosomy 8p23.1
- monosomy 8p23.1
