8p11.2 deletion syndrome
From BugSigDB
8p11.2 deletion syndrome is a contiguous gene syndrome characterized by the association of congenital spherocytosis, dysmorphic features, growth delay and hypogonadotropic hypogonadism.
- Aliases
- 8p11.2 deletion syndrome
- Del(8)(p11.2)
- Monosomy 8p11.2
- monosomy 8p11.2
