Z82.79

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 ambiguous genitalia

• Family history of anencephaly fetus with severely underdeveloped brain)

• Family history of anencephaly and neural tube defect

• Family history of autosomal aneuploidy

• Family history of autosomal aneuploidy abnormal number of chromosomes)

• Family history of autosomal translocation

• Family history of autosomal translocation abnormal structure of chromosomes)

• 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 with patient at risk

• 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 cowden syndrome

• Family history of cowden syndrome inherited skin disease)

• Family history of craniosynostosis

• Family history of craniosynostosis abnormal skull growth in infant)

• Family history of cystic hygroma

• Family history of cystic hygroma benign tumor)

• Family history of down syndrome inherited chromosome disorder)

• 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 osteogenesis imperfecta

• Family history of prader-willi syndrome

• Family history of prader-willi syndrome inherited chromosome disorder)

• 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 13

• Family history of trisomy 13 inherited chromosome disorder)

• Family history of trisomy 18

• Family history of trisomy 18 inherited chromosome disorder)

• Family history of trisomy 21 – down syndrome inherited chromosome disorder)

• Family history of trisomy 21 down syndrome

• Family history of turner syndrome

• Family history of turner syndrome 45, x) inherited chromosome disorder)

• 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)

• Fh: anencephaly

• Fh: chromosomal anomaly

• Fh: congenital anomaly

• Fh: spina bifida

Present On Admission

• Z82.79

Details

• Z82.79 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

• Short description: Fam hx of congen malform, deformations and chromsoml abnlt

• The 2023 edition of ICD-10-CM Z82.79 became effective on October 1, 2022.

• This is the American ICD-10-CM version of Z82.79 – other international versions of ICD-10 Z82.79 may differ.