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Z15.8
Genetic susceptibility to other disease
ICD10CM code
Similar Codes
ICD10CM codes
Z15.8
- Genetic susceptibility to other disease
Z15.89
- Genetic susceptibility to other disease
Z15
- Genetic susceptibility to disease
Z15.09
- Genetic susceptibility to other malignant neoplasm
Z14.8
- Genetic carrier of other disease
Z15.0
- Genetic susceptibility to malignant neoplasm
Z15.01
- Genetic susceptibility to malignant neoplasm of breast
Z15.03
- Genetic susceptibility to malignant neoplasm of prostate
Z84.81
- Family history of carrier of genetic disease
Z84.8
- Family history of other specified conditions
HCPCS codes
G8959
- Clinician treating major depressive disorder communicates to clinician treating comorbid condition
G8947
- One or more neuropsychiatric symptoms
G8972
- One or more high risk factors for thromboembolism or more than one moderate risk factor for thromboe
G0105
- Colorectal cancer screening; colonoscopy on individual at high risk
H1000
- Prenatal care, at-risk assessment
G9012
- Other specified case management service not elsewhere classified
G9416
- Patient had one tetanus, diphtheria toxoids and acellular pertussis vaccine (tdap) on or between the
G9560
- Patient not treated with a beta-lactam antibiotic as definitive therapy, reason not given
G9420
- Specimen site other than anatomic location of lung or is not classified as primary non-small cell lu
G9918
- Functional status not performed, reason not otherwise specified
CPT4 codes
81425
- Genome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis
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
87900
- Infectious agent drug susceptibility phenotype prediction using regularly updated genotypic bioinfor
81443
- Genetic testing for severe inherited conditions (eg, cystic fibrosis, Ashkenazi Jewish-associated di
81439
- Hereditary cardiomyopathy (eg, hypertrophic cardiomyopathy, dilated cardiomyopathy, arrhythmogenic r
0060U
- Twin zygosity, genomic targeted sequence analysis of chromosome 2, using circulating cell-free fetal
81471
- X-linked intellectual disability (XLID) (eg, syndromic and non-syndromic XLID); duplication/deletion
81416
- Exome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis, each co
81415
- Exome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis