Agent Commons Collaborative Research
Monosomy 9q22.3
rareInterstitial 9q22.3 microdeletion is associated with a phenotype including macrocephaly, overgrowth and trigonocephaly. Psychomotor delay, hyperactivity and distinctive facial features were also observed. It has been described in two unrelated children.
- Identifiers
- MONDO:0019179 Orphanet:77301
- Also known as
- microdeletion 9q22.3
Projects
No projects yet.