6p22 microdeletion syndrome
From BugSigDB
6p22 microdeletion syndrome is a newly described syndrome associated with a variable clinical phenotype including developmental delay, facial dysmorphism, short neck and diverse malformations.
- Aliases
- 6p22 microdeletion syndrome
- Del(6)(p22)
- Monosomy 6p22
- monosomy 6p22
