Z82.79
BillableFam hx of congen malform, deformations and chromsoml abnlt
Family history of other congenital malformations, deformations and chromosomal abnormalities
Coding Notes
Code Also
A second code may be required; sequencing depends on circumstances
Related Codes(1)
Also Known As / Clinical Terms(190)
SNOMED CT
- Family history of neoplasm of skin160288009
- FH: Obesity160311006
- Family history: Obesity160311006
- FH: Ear disorder160352002
- Family history of ear disorder160352002
- Family history: Ear disorder160352002
- FH: Congen heart disease160364005
- FH: Congenital heart disease160364005
- Family history: Congenital heart disease160364005
- Family history of congenital anomaly160417009
- Family history of congenital disease160417009
- FH: Anencephaly160418004
- Family history of anencephaly160418004
- Family history: Anencephaly160418004
- FH: Spina bifida160419007
- Family history of Spina bifida160419007
- Family history of neural tube defect160419007
- Family history: Spina bifida160419007
- FH: Congenital RS anomaly160421002
- Family history of congenital respiratory system anomaly160421002
- Family history: Congenital RS anomaly160421002
- FH: Congenital GIT anomaly160422009
- Family history: Congenital gastrointestinal tract anomaly160422009
- FH: Congenital GU anomaly160423004
- Family history: Congenital GU anomaly160423004
- Family history: Congenital genitourinary anomaly160423004
- FH: Cong. orthopaedic anomaly160424005
- FH: Cong. orthopedic anomaly160424005
- Family history: Congenital orthopaedic anomaly160424005
- Family history: Congenital orthopedic anomaly160424005
- Family history of chromosomal anomaly160425006
- FH: Congenital CVS anomaly266908007
- Family history of congenital anomaly of cardiovascular system266908007
- Family history: Congenital CVS anomaly266908007
- Family history of Down syndrome281022002
- Family history of complete trisomy 21 syndrome281022002
- FH: - kidney disorder289916006
- FH: Kidney disorder289916006
- FH: Renal disorder289916006
- Family history of kidney disease289916006
- Maternal history of congenital dislocated hip413308009
- Family history of pulmonary infundibular stenosis417648007
- Family history of aortic stenosis429952000
- Family history of stenosis of aortic valve429952000
- Family history of cleft lip429954004
- Family history of cleft palate430086009
- Family history of nephrotic syndrome430808009
- Family history of cleft lip and cleft palate433279009
- Family history of cleft palate with cleft lip433279009
- Family history of congenital hip dysplasia700191004
- Family history of intellectual development disorder763598005
- Family history of intellectual disability763598005
- Family history of congenital microcephalus1148759006
- Family history of congenital microcephaly1148759006
- Family history of Cowden syndrome65031000119108
- Family history of Marfan syndrome64181000119106
- Family history of Prader-Willi syndrome64851000119105
- Family history of Turner syndrome64861000119107
- Family history of VUR - vesicoureteral reflux430081000124104
- Family history of vesicoureteral reflux430081000124104
- Family history of achondroplasia64121000119107
- Family history of ambiguous genitalia64651000119109
- Family history of autosomal aneuploidy65011000119103
- Family history of autosomal translocation144171000119108
- Family history of complex congenital heart disease64041000119100
- Family history of congenital Finnish nephrotic syndrome76531000119104
- Family history of congenital anomaly of ear64681000119102
- Family history of congenital diaphragmatic hernia6900001000004102
- Family history of congenital hydrocephalus63941000119102
- Family history of congenital malformation597941000005106
- Family history of congenital stenosis of aorta6830001000004103
- Family history of craniosynostosis94721000119105
- Family history of cystic hygroma64911000119103
- Family history of disorder due to sex chromosome abnormality286501000119106
- Family history of disorder of skeletal and/or smooth muscle456781000124103
- Family history of myopathy456781000124103
- Family history of dysmorphism456671000124106
- Family history of fragile X syndrome65071000119106
- Family history of holoprosencephaly6820001000004100
- Family history of hypospadias71201000119102
- Family history of macrocephaly94741000119104
- Family history of microcephaly94761000119100
- Family history of multiple congenital anomalies64731000119106
- Family history of neurofibromatosis65021000119105
- Family history of osteogenesis imperfecta98041000119107
- Family history of sex chromosome aneuploidy64921000119105
- Family history of sex chromosome translocation64931000119108
- Family history of short stature69731000119107
- Family history of single congenital anomaly85951000119104
- Family history of transposition of great vessels7100001000004100
- Family history of trisomy 1364831000119104
- Family history of trisomy 1864841000119108
- Family history of trisomy 18 syndrome6810001000004108
- Family history of velocardiofacial syndrome64991000119107
UMLS
Clinical Terms
- Family history of kidney disease
- Family history: Congenital genitourinary anomaly
- Family history of congenital anomaly
- Family history of congenital microcephalus
- FH: Ear disorder
- Family history of dysmorphism
- Family history of complex congenital heart disease
- Family history of Down syndrome
- Family history of congenital respiratory system anomaly
- Family history: Congenital GU anomaly
- Family history of anencephaly
- Family history of intellectual disability
- FH: Congenital GU anomaly
- Family history of congenital disease
- FH: - kidney disorder
- FH: Kidney disorder
- Family history of neural tube defect
- FH: Congenital GIT anomaly
- Family history of osteogenesis imperfecta
- Family history of nephrotic syndrome
- Family history of pulmonary infundibular stenosis
- FH: Congenital heart disease
- Family history of myopathy
- Family history of Spina bifida
- Family history of trisomy 18 syndrome
- Family history of congenital hydrocephalus
- Family history of sex chromosome aneuploidy
- Family history of aortic stenosis
- Family history of autosomal translocation
- Maternal history of congenital dislocated hip
- FH: Congen heart disease
- Family history of neoplasm of skin
- Family history: Spina bifida
- Family history of congenital microcephaly
- FH: Obesity
- Family history of congenital stenosis of aorta
- FH: Spina bifida
- Family history of vesicoureteral reflux
- Family history of neurofibromatosis
- Family history: Anencephaly
- Family history of cleft palate
- Family history of VUR - vesicoureteral reflux
- FH: Congenital RS anomaly
- Family history of Cowden syndrome
- Family history of disorder of skeletal and/or smooth muscle
- Family history of trisomy 13
- Family history of microcephaly
- Family history: Congenital RS anomaly
- Family history: Congenital gastrointestinal tract anomaly
- Family history: Obesity
- Family history of Marfan syndrome
- Family history of holoprosencephaly
- Family history of disorder due to sex chromosome abnormality
- Family history of congenital diaphragmatic hernia
- Family history of congenital anomaly of ear
- Family history of cleft lip and cleft palate
- Family history of stenosis of aortic valve
- Family history of cleft lip
- FH: Anencephaly
- Family history of chromosomal anomaly
- Family history of congenital malformation
- Family history of transposition of great vessels
- Family history of complete trisomy 21 syndrome
- Family history of fragile X syndrome
- Family history of cleft palate with cleft lip
- FH: Cong. orthopedic anomaly
- Family history of intellectual development disorder
- Family history of achondroplasia
- Family history of short stature
- FH: Cong. orthopaedic anomaly
- Family history of macrocephaly
- Family history: Congenital orthopedic anomaly
- Family history of single congenital anomaly
- Family history of congenital hip dysplasia
- Family history of sex chromosome translocation
- Family history of congenital anomaly of cardiovascular system
- Family history of Turner syndrome
- Family history of congenital Finnish nephrotic syndrome
- Family history of cystic hygroma
- Family history of ear disorder
- Family history of trisomy 18
- FH: Renal disorder
- Family history of hypospadias
- FH: Congenital CVS anomaly
- Family history of Prader-Willi syndrome
- Family history of autosomal aneuploidy
- Family history: Ear disorder
- Family history: Congenital CVS anomaly
- Family history: Congenital heart disease
- Family history: Congenital orthopaedic anomaly
- Family history of multiple congenital anomalies
- Family history of velocardiofacial syndrome
- Family history of craniosynostosis
- Family history of ambiguous genitalia
Frequently Asked Questions
What is the ICD-10 code for fam hx of congen malform, deformations and chromsoml abnlt?
The ICD-10-CM code for fam hx of congen malform, deformations and chromsoml abnlt is Z82.79. The full clinical description is "Family history of other congenital malformations, deformations and chromosomal abnormalities". Z82.79 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Z82.79 mean?
ICD-10-CM code Z82.79 represents “Family history of other congenital malformations, deformations and chromosomal abnormalities”. It is classified under Chapter 22: Factors Influencing Health Status and Contact With Health Services and is a billable/specific code that can be used on a claim.
Is Z82.79 a billable code?
Yes, Z82.79 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Z82.79 in?
Z82.79 is in Chapter 22: Factors Influencing Health Status and Contact With Health Services (codes Z00-Z99).
What SNOMED CT codes does Z82.79 map to?
Z82.79 maps to 63 SNOMED CT concepts: 289916006, 160418004, 160424005, 160364005, 266908007, and 58 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Z82.79?
Z82.79 is linked to 1 UMLS Concept Unique Identifier: C2911235. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Z82.79 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like fam hx of congen malform, deformations and chromsoml abnlt affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of Z82.79?
There is no direct ICD-11 mapping available for Z82.79 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.