Diagnosis Code: Z82.79

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

Long Description: Family history of other congenital malformations, deformations and chromosomal abnormalities

The code Z82.79 is VALID for claim submission

Code Classification:

• Factors influencing health status and contact with health services (Z00–Z99)
  • Persons with potential health hazards related to family and personal history and certain conditions influencing health status (Z77-Z99)
    • Fam hx of certain disabil & chr dis (leading to disablement) (Z82)
      • Z82.79 Fam hx of congen malform, deformations and chromsoml abnlt

This code is valid for unacceptable principal diagnosis

Code Version: 2022 ICD-10-CM

Synonyms

• Family history of achondroplasia
• Family history of ambiguous genitalia
• Family history of anencephaly
• Family history of autosomal aneuploidy
• Family history of autosomal translocation
• Family history of chromosomal anomaly
• Family history of cleft lip
• Family history of cleft palate
• Family history of cleft palate with cleft lip
• Family history of complete trisomy 21 syndrome
• Family history of complex congenital heart disease
• Family history of congenital anomaly of cardiovascular system
• Family history of congenital anomaly of cardiovascular system
• Family history of congenital anomaly of cardiovascular system
• Family history of congenital anomaly of cardiovascular system
• Family history of congenital anomaly of cardiovascular system
• Family history of congenital anomaly of ear
• Family history of congenital diaphragmatic hernia
• Family history of congenital disease
• Family history of congenital Finnish nephrotic syndrome
• Family history of congenital hip dysplasia
• Family history of congenital hydrocephalus
• Family history of congenital microcephaly
• Family history of congenital stenosis of aorta
• Family history of Cowden syndrome
• Family history of craniosynostosis
• Family history of cystic hygroma
• Family history of disorder due to sex chromosome abnormality
• Family history of disorder of skeletal and/or smooth muscle
• Family history of dysmorphism
• Family history of fragile X syndrome
• Family history of holoprosencephaly
• Family history of hypospadias
• Family history of intellectual disability
• Family history of kidney disease
• Family history of macrocephaly
• Family history of Marfan syndrome
• Family history of microcephaly
• Family history of multiple congenital anomalies
• Family history of nephrotic syndrome
• Family history of neurofibromatosis
• Family history of osteogenesis imperfecta
• Family history of Prader-Willi syndrome
• Family history of pulmonary infundibular stenosis
• Family history of sex chromosome aneuploidy
• Family history of sex chromosome translocation
• Family history of short stature
• Family history of single congenital anomaly
• Family history of Spina bifida
• Family history of stenosis of aortic valve
• Family history of transposition of great vessels
• Family history of trisomy 13
• Family history of trisomy 18
• Family history of trisomy 18 syndrome
• Family history of Turner syndrome
• Family history of velocardiofacial syndrome
• Family history of vesicoureteral reflux
• FH: Cong. orthopedic anomaly
• FH: Congenital GIT anomaly
• FH: Congenital GU anomaly
• FH: Congenital GU anomaly
• FH: Congenital heart disease
• FH: Congenital RS anomaly
• FH: Ear disorder
• FH: neoplasm of skin
• Maternal history of congenital dislocated hip

Crosswalk Information

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This page was last updated on: 10/1/2023

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