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Z82.7
Family history of congenital malformations, deformations and chromosomal abnormalities
ICD10CM code
Similar Codes
ICD10CM codes
Z82.7
- Family history of congenital malformations, deformations and chromosomal abnormalities
Z82.79
- Family history of other congenital malformations, deformations and chromosomal abnormalities
Z87.7
- Personal history of (corrected) congenital malformations
Z87.79
- Personal history of other (corrected) congenital malformations
Z87.798
- Personal history of other (corrected) congenital malformations
Z87.72
- Personal history of (corrected) congenital malformations of nervous system and sense organs
Z87.76
- Personal history of (corrected) congenital malformations of integument, limbs and musculoskeletal sy
Z84.81
- Family history of carrier of genetic disease
Z87.74
- Personal history of (corrected) congenital malformations of heart and circulatory system
Z87.728
- Personal history of other specified (corrected) congenital malformations of nervous system and sense
HCPCS codes
G8972
- One or more high risk factors for thromboembolism or more than one moderate risk factor for thromboe
H1000
- Prenatal care, at-risk assessment
C8921
- Transthoracic echocardiography with contrast, or without contrast followed by with contrast, for con
G9318
- Imaging study named according to standardized nomenclature
G9597
- Pediatric patient with minor blunt head trauma not classified as low risk according to the pecarn pr
G9593
- Pediatric patient with minor blunt head trauma classified as low risk according to the pecarn predic
G8947
- One or more neuropsychiatric symptoms
G9416
- Patient had one tetanus, diphtheria toxoids and acellular pertussis vaccine (tdap) on or between the
S9435
- Medical foods for inborn errors of metabolism
G9618
- Documentation of screening for uterine malignancy or those that had an ultrasound and/or endometrial
CPT4 codes
81508
- Fetal congenital abnormalities, biochemical assays of two proteins (PAPP-A, hCG [any form]), utilizi
81422
- Fetal chromosomal microdeletion(s) genomic sequence analysis (eg, DiGeorge syndrome, Cri-du-chat syn
81512
- Fetal congenital abnormalities, biochemical assays of five analytes (AFP, uE3, total hCG, hyperglyco
93530
- Right heart catheterization, for congenital cardiac anomalies
81425
- Genome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis
0060U
- Twin zygosity, genomic targeted sequence analysis of chromosome 2, using circulating cell-free fetal
81511
- Fetal congenital abnormalities, biochemical assays of four analytes (AFP, uE3, hCG [any form], DIA)
88280
- Chromosome analysis; additional karyotypes, each study
88289
- Chromosome analysis; additional high resolution study
93303
- Transthoracic echocardiography for congenital cardiac anomalies; complete