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Genetic carrier of other disease

ICD10CM code

Medical Policies and Guidelines for Genetic carrier of other disease

Related policies from health plans

Vyondys 53 (golodirsen)
Prenatal Testing (CG043)
Concert Genetic Testing: Preimplantation Genetic Testing (PDF)
Concert Genetic Testing: Prenatal Diagnosis Pregnancy Loss (PDF)
Concert Genetic Testing: Prenatal Diagnosis Pregnancy Loss (PDF)

Similar Codes


ICD10CM codes

Z14.8 - Genetic carrier of other disease
Z14 - Genetic carrier
Z84.81 - Family history of carrier of genetic disease
Z15.8 - Genetic susceptibility to other disease
Z15.89 - Genetic susceptibility to other disease
Z22.8 - Carrier of other infectious diseases
Z22.3 - Carrier of other specified bacterial diseases
Z84.8 - Family history of other specified conditions
Z22.39 - Carrier of other specified bacterial diseases
Z14.1 - Cystic fibrosis carrier

HCPCS codes

G9012 - Other specified case management service not elsewhere classified
G8959 - Clinician treating major depressive disorder communicates to clinician treating comorbid condition
G9842 - Patient has metastatic disease at diagnosis
G9918 - Functional status not performed, reason not otherwise specified
G8972 - One or more high risk factors for thromboembolism or more than one moderate risk factor for thromboe
G9420 - Specimen site other than anatomic location of lung or is not classified as primary non-small cell lu
D0190 - Screening of a patient
H1000 - Prenatal care, at-risk assessment
D9450 - CASE PRESENTATION
G9902 - Patient screened for tobacco use and identified as a tobacco user

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
0060U - Twin zygosity, genomic targeted sequence analysis of chromosome 2, using circulating cell-free fetal
81443 - Genetic testing for severe inherited conditions (eg, cystic fibrosis, Ashkenazi Jewish-associated di
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
81471 - X-linked intellectual disability (XLID) (eg, syndromic and non-syndromic XLID); duplication/deletion
81415 - Exome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis
88289 - Chromosome analysis; additional high resolution study