Specific code 2012 ICD-9-CM Diagnosis Code V19.5
Family history of congenital anomalies
  • Short description: Fam hx-congen anomalies.
  • ICD-9-CM V19.5 will be replaced by an equivalent ICD-10-CM code (or codes) when the United States transitions from ICD-9-CM to ICD-10-CM on October 1, 2015.
  • ICD-9-CM V19.5 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 V19.5.
  • More recent version(s) of ICD-9-CM V19.5: 2013 2014.
Disease Synonyms
  • Down's child in family
  • Family history of abdominal wall defect
  • Family history of achondroplasia
  • Family history of achondroplasia (type of dwarfism)
  • Family history of anencephaly (fetus with severely underdeveloped brain)
  • Family history of anencephaly and neural tube defect
  • Family history of autosomal translocation
  • Family history of autosomal translocation (abnormal structure of chromosomes)
  • Family history of chromosomal abnormality
  • Family history of chromosomal disorder
  • Family history of cleft lip
  • Family history of cleft palate
  • Family history of clubfoot
  • Family history of complex congenital heart defect
  • Family history of complex congenital heart disease
  • Family history of congenital anomaly
  • Family history of congenital anomaly of ear
  • Family history of congenital ear anomaly
  • Family history of congenital Finish nephrosis
  • Family history of congenital Finnish nephrosis (kidney disease)
  • Family history of congenital hydrocephalus
  • Family history of congenital hydrocephalus (water on the brain)
  • Family history of congenital osteogenesis imperfecta
  • Family history of congenital osteogenesis imperfecta (brittle bones)
  • Family history of craniosynostosis
  • Family history of craniosynostosis (abnormal skull growth in infant)
  • Family history of Down syndrome (inherited chromosome disorder)
  • Family history of familial dysautonomia
  • Family history of familial dysautonomia (malfunction of part of nervous system)
  • Family history of fragile X
  • Family history of fragile X (inherited chromosome abnormality)
  • Family history of hypospadias (abnormal opening of penis)
  • Family history of hypospadius
  • Family history of macrocephaly
  • Family history of macrocephaly (large head)
  • Family history of Marfan syndrome
  • Family history of Marfan syndrome (disorder of connective tissue)
  • Family history of microcephaly
  • Family history of microcephaly (small head)
  • Family history of multiple congenital anomalies
  • Family history of neural tube defect, spina bifida
  • Family history of sex chromosome aneuploidy
  • Family history of sex chromosome aneuploidy (abnormal number of chromosomes)
  • Family history of sex chromosome disorder
  • Family history of sex chromosome translocation
  • Family history of sex chromosome translocation (abnormal structure of chromosomes)
  • Family history of single congenital anomaly
  • Family history of trisomy 21 - Down syndrome (inherited chromosome disorder)
  • Family history of trisomy 21 down syndrome
  • Family history of velocardiofacial syndrome
  • Family history of velocardiofacial syndrome (inherited chromosome disorder)
  • Family history of Von Hippel-Lindau syndrome
  • Family history of von Hippel-Lindau syndrome (inherited chromosome disorder)
  • Family history: Congenital anomaly
  • Family history: Spina bifida
  • FH: Congenital anomaly
  • FH: Spina bifida
  • Fhx of abdominal wall defect
  • Fhx of achondroplasia
  • Fhx of anencephaly neural tube defect
  • Fhx of autosomal translocation
  • Fhx of chromosomal abnormality
  • Fhx of cleft lip
  • Fhx of cleft palate
  • Fhx of clubfoot
  • Fhx of complex congenital heart defect
  • Fhx of congenital anomaly
  • Fhx of congenital ear anomaly
  • Fhx of congenital finnish nephrosis
  • Fhx of congenital hydrocephalus
  • Fhx of congenital osteogenesis imperfecta
  • Fhx of craniosynostosis
  • Fhx of Down syndrome
  • Fhx of familial dysautonomia
  • Fhx of fragile x
  • Fhx of hypospadias
  • Fhx of macrocephaly
  • Fhx of marfan syndrome
  • Fhx of microcephaly
  • Fhx of multiple congenital anomalies
  • Fhx of sex chromosome aneuploidy
  • Fhx of sex chromosome disorder
  • Fhx of sex chromosome translocation
  • Fhx of single congenital anomaly
  • Fhx of spina bifida
  • Fhx of trisomy 21 Down syndrome
  • Fhx of velocardiofacial syndrome
  • Fhx of von Hippel-Lindau syndrome
Convert to ICD-10-CM: V19.5 converts directly to:
  • 2014 ICD-10-CM Z82.79 Family history of other congenital malformations, deformations and chromosomal abnormalities
ICD-9-CM Volume 2 Index entries containing back-references to V19.5:
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM V19.5 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2012 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.