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Z15
Genetic susceptibility to disease
ICD10CM code
Medical Policies and Guidelines for Genetic susceptibility to disease
Related policies from health plans
SUNFLOWER
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