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
- any follow-up examination (Z08-Z09)
Also Known As / Clinical Terms
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
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.
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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.