758.32 is a billable ICD-9-CM medical code that can be used to specify a diagnosis on a reimbursement claim.
Diagnosis Definition(s)
Typical facies with a prominent nose and retruded mandible, cleft palate, cardiovascular defects, learning disability, retarded mental development, and short stature. Elements of this syndrome are frequently present in the Robin syndrome.
caused by microdeletion on chromosome 22q11.2; associated with multiple congenital anomalies, learning disabilities, behavioral phenotypes including ADHD and anxiety, with schizophrenic risk in adulthood.
Also applicable to/known as
Deletion 22q11.2
ICD-9-CM Volume 2 Index Entries That Refer To 758.32
2010 ICD-9-CM Diagnosis Code 758.32
758.32