Catalog

8p23.1 deletion

No MMS code

Link to WHO Definition

8p23.1 deletion – http://id.who.int/icd/entity/933685931

8p23.1 deletion involves a partial deletion of the short arm of chromosome 8 characterised by low birth weight, postnatal growth deficiency, mild intellectual deficit, hyperactivity, craniofacial abnormalities, and congenital heart defects.