Home > 2014 ICD-10-CM Diagnosis Codes > Congenital malformations, deformations and chromosomal abnormalities Q00-Q99 > Other congenital malformations Q80-Q89 > Congenital malformation syndromes due to known exogenous causes, not elsewhere classified Q86-
2014 ICD-10-CM Diagnosis Code Q86.2
Dysmorphism due to warfarin
Q86.2 is a specific ICD-10-CM diagnosis code that can be used to specify a diagnosis.
ICD-9-CM will be replaced by ICD-10-CM beginning October 1, 2014, therefore, Q86.2 and all other ICD-10-CM diagnosis codes should only be used for training or planning purposes until then.
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.
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.gov]
ICD-10 Q86.2 as underlying cause of death data broken down by: gender, age, race, year
ICD-10-CM Q86.2 is part of Diagnostic Related Group (MS-DRG v30.0):