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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