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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