Specific code icon 2015 ICD-10-CM Diagnosis Code Q86.2

Dysmorphism due to warfarin

    2015 Billable Code POA Exempt

  • Q86.2 is a billable ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
  • On October 1, 2015 ICD-10-CM will replace ICD-9-CM in the United States, therefore, Q86.2 - and all other ICD-10-CM codes - should only be used for training or planning purposes until then.
  • This is the American ICD-10-CM version of Q86.2. Other international ICD-10 versions may differ.

Clinical Information
  • A rare syndrome characterized by congenital abnormalities caused by fetal exposure to the administration of warfarin to the mother during pregnancy. The congenital abnormalities include nasal bridge depression, nasal bones hypoplasia, microcephaly, congenital heart disorders, and brachydactyly.
  • Multiple abnormalities in infants whose mother were treated with coumarin anticoagulants during pregnancy. The most common anomalies include developmental delay, neurological complications (usually hydrocephalus and occasional agenesis of the corpus callosum and meningoencephalocele), midfacial hypoplasia, and various ocular, skeletal, and other defects.
Present On Admission
  • Q86.2 is considered exempt from POA reporting.
ICD-10-CM Q86.2 is grouped within Diagnostic Related Group (MS-DRG v30.0):
  • 794 Neonate with other significant problems

Convert ICD-10-CM Q86.2 to ICD-9-CM

The following ICD-10-CM Index entries contain back-references to ICD-10-CM Q86.2: