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Genetic susceptibility to other disease

ICD10CM code

Medical Policies and Guidelines for Genetic susceptibility to other disease

Related policies from health plans

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