Specific code icon 2014 ICD-10-CM Diagnosis Code Q86.2

Dysmorphism due to warfarin

  • Q86.2 is a billable ICD-10-CM code that can be used to specify a diagnosis.
  • 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.
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.
Mortality Data
  • Between 1999-2007 there was 1 death in the United States where ICD-10 Q86.2 was indicated as the underlying cause of death [source: cdc.govlink to cdc.gov]
  • ICD-10 Q86.2 as underlying cause of death data broken down by: gender, age, race, year
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: