Specific code icon 2015 ICD-10-CM Diagnosis Code Z82.79

Family history of other congenital malformations, deformations and chromosomal abnormalities

    2015 Billable Code Unacceptable As Principal Dx POA Exempt

  • Z82.79 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, Z82.79 - 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 Z82.79. Other international ICD-10 versions may differ.

Description Synonyms
  • Down's child in family
  • Down's child in family (situation)
  • Family history of abdominal wall defect
  • Family history of abdominal wall defect (situation)
  • Family history of achondroplasia
  • Family history of achondroplasia (situation)
  • Family history of achondroplasia (type of dwarfism)
  • Family history of ambiguous genitalia
  • Family history of ambiguous genitalia (situation)
  • Family history of anencephaly (fetus with severely underdeveloped brain)
  • Family history of anencephaly and neural tube defect
  • Family history of anencephaly and neural tube defect (situation)
  • Family history of autosomal aneuploidy
  • Family history of autosomal aneuploidy (abnormal number of chromosomes)
  • Family history of autosomal aneuploidy (situation)
  • Family history of autosomal translocation
  • Family history of autosomal translocation (abnormal structure of chromosomes)
  • Family history of autosomal translocation (situation)
  • Family history of chromosomal abnormality
  • Family history of chromosomal abnormality with the patient or offspring at risk
  • Family history of chromosomal disorder
  • Family history of chromosomal disorder (situation)
  • Family history of chromosomal disorder with patient at risk
  • Family history of chromosomal disorder with patient at risk (situation)
  • Family history of cleft lip
  • Family history of cleft lip (situation)
  • Family history of cleft palate
  • Family history of cleft palate (situation)
  • Family history of clubfoot
  • Family history of clubfoot (situation)
  • Family history of complex congenital heart defect
  • Family history of complex congenital heart disease
  • Family history of complex congenital heart disease (situation)
  • Family history of congenital anomaly
  • Family history of congenital anomaly of ear
  • Family history of congenital anomaly of ear (situation)
  • Family history of congenital ear anomaly
  • Family history of congenital Finish nephrosis
  • Family history of congenital Finish nephrosis (situation)
  • Family history of congenital Finnish nephrosis (kidney disease)
  • Family history of congenital hydrocephalus
  • Family history of congenital hydrocephalus (situation)
  • 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 congenital osteogenesis imperfecta (situation)
  • Family history of Cowden syndrome
  • Family history of Cowden syndrome (inherited skin disease)
  • Family history of Cowden syndrome (situation)
  • Family history of craniosynostosis
  • Family history of craniosynostosis (abnormal skull growth in infant)
  • Family history of craniosynostosis (situation)
  • Family history of cystic hygroma
  • Family history of cystic hygroma (benign tumor)
  • Family history of cystic hygroma (situation)
  • Family history of Down syndrome (inherited chromosome disorder)
  • Family history of fragile X
  • Family history of fragile X (inherited chromosome abnormality)
  • Family history of fragile X (situation)
  • Family history of hypospadias (abnormal opening of penis)
  • Family history of hypospadius
  • Family history of hypospadius (situation)
  • Family history of macrocephaly
  • Family history of macrocephaly (large head)
  • Family history of macrocephaly (situation)
  • Family history of Marfan syndrome
  • Family history of Marfan syndrome (disorder of connective tissue)
  • Family history of Marfan syndrome (situation)
  • Family history of microcephaly
  • Family history of microcephaly (situation)
  • Family history of microcephaly (small head)
  • Family history of multiple congenital anomalies
  • Family history of multiple congenital anomalies (situation)
  • Family history of neural tube defect, spina bifida
  • Family history of Prader-Willi syndrome
  • Family history of Prader-Willi syndrome (inherited chromosome disorder)
  • Family history of Prader-Willi syndrome (situation)
  • Family history of sex chromosome aneuploidy
  • Family history of sex chromosome aneuploidy (abnormal number of chromosomes)
  • Family history of sex chromosome aneuploidy (situation)
  • Family history of sex chromosome disorder
  • Family history of sex chromosome disorder (situation)
  • Family history of sex chromosome translocation
  • Family history of sex chromosome translocation (abnormal structure of chromosomes)
  • Family history of sex chromosome translocation (situation)
  • Family history of single congenital anomaly
  • Family history of single congenital anomaly (situation)
  • Family history of trisomy 13
  • Family history of trisomy 13 (inherited chromosome disorder)
  • Family history of trisomy 13 (situation)
  • Family history of trisomy 18
  • Family history of trisomy 18 (inherited chromosome disorder)
  • Family history of trisomy 18 (situation)
  • Family history of trisomy 21 - Down syndrome (inherited chromosome disorder)
  • Family history of trisomy 21 down syndrome
  • Family history of trisomy 21 down syndrome (situation)
  • Family history of Turner syndrome
  • Family history of Turner syndrome (45, X) (inherited chromosome disorder)
  • Family history of Turner syndrome (situation)
  • Family history of velocardiofacial syndrome
  • Family history of velocardiofacial syndrome (inherited chromosome disorder)
  • Family history of velocardiofacial syndrome (situation)
  • Family history of Von Hippel-Lindau syndrome
  • Family history of von Hippel-Lindau syndrome (inherited chromosome disorder)
  • Family history of Von Hippel-Lindau syndrome (situation)
  • Family history: Anencephaly (situation)
  • Family history: Congenital anomaly (situation)
  • Family history: Spina bifida (situation)
  • FH: Anencephaly
  • FH: Congenital anomaly
  • FH: Spina bifida
  • Fhx of abdominal wall defect
  • Fhx of achondroplasia
  • Fhx of ambiguous genitalia
  • Fhx of anencephaly
  • Fhx of anencephaly neural tube defect
  • Fhx of autosomal aneuploidy
  • Fhx of autosomal translocation
  • Fhx of chromosomal abnormality
  • Fhx of chromosomal abnormality at risk
  • 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 cowden syndrome
  • Fhx of craniosynostosis
  • Fhx of cystic hygroma
  • Fhx of Down syndrome
  • Fhx of fragile x
  • Fhx of hypospadias
  • Fhx of macrocephaly
  • Fhx of marfan syndrome
  • Fhx of microcephaly
  • Fhx of multiple congenital anomalies
  • Fhx of Prader-Willi syndrome
  • 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 13
  • Fhx of trisomy 18
  • Fhx of trisomy 21 Down syndrome
  • Fhx of Turner syndrome (45,X)
  • Fhx of velocardiofacial syndrome
  • Fhx of von Hippel-Lindau syndrome
ICD-10-CM Coding Rules
  • Z82.79 is considered unacceptable as a principal diagnosis as it describes a circumstance which influences an individual's health status but not a current illness or injury, or the diagnosis may not be a specific manifestation but may be due to an underlying cause.
Present On Admission
  • Z82.79 is considered exempt from POA reporting.
ICD-10-CM Z82.79 is grouped within Diagnostic Related Group (MS-DRG v30.0):
  • 951 Other factors influencing health status

Convert ICD-10-CM Z82.79 to ICD-9-CM

The following ICD-10-CM Index entries contain back-references to ICD-10-CM Z82.79: