2010 ICD-9-CM Diagnosis Code V19.5
Family history of congenital anomalies
- Short description: Fam hx-congen anomalies.
- ICD-9-CM V19.5 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, V19.5 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
- You are viewing the 2010 version of ICD-9-CM V19.5.
- More recent version(s) of ICD-9-CM V19.5: 2011 2012 2013 2014 2015.
Convert to ICD-10-CM:
V19.5 converts directly to:
- 2015/16 ICD-10-CM Z82.79 Family history of other congenital malformations, deformations and chromosomal abnormalities
Approximate 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 hereditary disease
- Family history of heritable disorder
- 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 heritable disorder
- 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
ICD-9-CM Volume 2 Index entries containing back-references to
V19.5:
- History (personal) of
family
allergy V19.6
