2012 ICD-9-CM Diagnosis Code 758.2
- A syndrome characterized by the presence of an extra (third) chromosome on an otherwise diploid chromosome 18 associated with a broad spectrum of variable abnormalities consisting of more than 130 individual defects of the craniofacial structures, brain, heart, kidneys, and gut. One-third of newborn infants (weighing about 2300) are premature and two-thirds are female. Fetal abnormalities consist mainly of polyhydramnios, small placenta, and single umbilical artery. Tumors in some cases. Trisomy 18 mosaicism is often associated with normal intelligence and mild phenotype.
- ICD-9-CM 758.2 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
- You are viewing the 2012 version of ICD-9-CM 758.2.
- More recent version(s) of ICD-9-CM 758.2: 2013.
Convert 758.2 to ICD-10-CM
ICD-9-CM Volume 2 Index entries containing back-references to 758.2: