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Z15.89
Genetic susceptibility to other disease
ICD10CM code
Medical Policies and Guidelines for Genetic susceptibility to other disease
Related policies from health plans
SUNFLOWER
Concert Genetic Testing: General Approach to Genetic Testing (PDF)
Similar Codes
ICD10CM codes
Z15.89
- Genetic susceptibility to other disease
Z15.8
- 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
Z84.81
- Family history of carrier of genetic disease
Z84.89
- Family history of other specified conditions
Z15.01
- Genetic susceptibility to malignant neoplasm of breast
Z15.03
- Genetic susceptibility to malignant neoplasm of prostate
HCPCS codes
G8959
- Clinician treating major depressive disorder communicates to clinician treating comorbid condition
G8947
- One or more neuropsychiatric symptoms
H1000
- Prenatal care, at-risk assessment
D0190
- Screening of a patient
G9012
- Other specified case management service not elsewhere classified
A9900
- Miscellaneous dme supply, accessory, and/or service component of another hcpcs code
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
D0191
- Assessment of a patient
J3485
- Injection, zidovudine, 10 mg
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
88289
- Chromosome analysis; additional high resolution study
81415
- Exome (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
81416
- Exome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis, each co
87910
- Infectious agent genotype analysis by nucleic acid (DNA or RNA); cytomegalovirus