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Genetic susceptibility to disease

ICD10CM code

Medical Policies and Guidelines for Genetic susceptibility to disease

Related policies from health plans

Concert Genetic Testing: Prenatal and Preconception Carrier Screening (PDF)

Similar Codes


ICD10CM codes

Z15 - Genetic susceptibility to disease
Z15.8 - Genetic susceptibility to other disease
Z15.89 - Genetic susceptibility to other disease
Z15.0 - Genetic susceptibility to malignant neoplasm
Z15.09 - Genetic susceptibility to other malignant neoplasm
Z15.01 - Genetic susceptibility to malignant neoplasm of breast
Z15.03 - Genetic susceptibility to malignant neoplasm of prostate
Z14 - Genetic carrier
Z14.8 - Genetic carrier of other disease
Z84.81 - Family history of carrier of genetic disease

HCPCS codes

G9931 - Documentation of cha2ds2-vasc risk score of 0 or 1
G0105 - Colorectal cancer screening; colonoscopy on individual at high risk
S0265 - Genetic counseling, under physician supervision, each 15 minutes
H1000 - Prenatal care, at-risk assessment
J3485 - Injection, zidovudine, 10 mg
D0190 - Screening of a patient
G9416 - Patient had one tetanus, diphtheria toxoids and acellular pertussis vaccine (tdap) on or between the
J3399 - Injection, onasemnogene abeparvovec-xioi, per treatment, up to 5x10^15 vector genomes
G8947 - One or more neuropsychiatric symptoms
D0191 - Assessment of a patient

CPT4 codes

81412 - Ashkenazi Jewish associated disorders (eg, Bloom syndrome, Canavan disease, cystic fibrosis, familia
81470 - X-linked intellectual disability (XLID) (eg, syndromic and non-syndromic XLID); genomic sequence ana
81425 - Genome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis
87900 - Infectious agent drug susceptibility phenotype prediction using regularly updated genotypic bioinfor
0060U - Twin zygosity, genomic targeted sequence analysis of chromosome 2, using circulating cell-free fetal
81439 - Hereditary cardiomyopathy (eg, hypertrophic cardiomyopathy, dilated cardiomyopathy, arrhythmogenic r
81443 - Genetic testing for severe inherited conditions (eg, cystic fibrosis, Ashkenazi Jewish-associated di
81471 - X-linked intellectual disability (XLID) (eg, syndromic and non-syndromic XLID); duplication/deletion
81263 - IGH@ (Immunoglobulin heavy chain locus) (eg, leukemia and lymphoma, B-cell), variable region somatic
81415 - Exome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis