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Family history of carrier of genetic disease

ICD10CM code

Medical Policies and Guidelines for Family history of carrier of genetic disease

Related policies from health plans

Genetic Testing for Inherited Diseases
Genetic Testing for Inherited Diseases
Genetic Testing for Inherited Diseases
Genetic Testing for TP53 Mutations
Pharmacogenetic Testing
Iron Studies - (0568)
Iron Studies - (0568)
Iron Studies - (0568)
Iron Studies - (0568)
Prenatal Testing (CG043)
CG-GENE-13 Genetic Testing for Inherited Diseases
CG-GENE-13 Genetic Testing for Inherited Diseases
CG-GENE-13 Genetic Testing for Inherited Diseases
CG-GENE-18 Genetic Testing for TP53 Mutations
Transthoracic Echocardiography in Children - (0523)
Concert Genetic Testing: Epilepsy Neurodegenerative and Neuromuscular Conditions (PDF)
Concert Genetic Testing: Epilepsy Neurodegenerative and Neuromuscular Conditions (PDF)
Concert Genetic Testing: Cardiac Disorders (PDF)
Concert Genetic Testing: Cardiac Disorders (PDF)
Concert Genetic Testing: Epilepsy Neurodegenerative and Neuromuscular Conditions (PDF)

Similar Codes


ICD10CM codes

Z84.81 - Family history of carrier of genetic disease
Z14.8 - Genetic carrier of other disease
Z84.89 - Family history of other specified conditions
Z84.8 - Family history of other specified conditions
Z14 - Genetic carrier
Z84 - Family history of other conditions
Z83 - Family history of other specific disorders
Z82.79 - Family history of other congenital malformations, deformations and chromosomal abnormalities
Z82.7 - Family history of congenital malformations, deformations and chromosomal abnormalities
Z15.89 - Genetic susceptibility to other disease

HCPCS codes

G8972 - One or more high risk factors for thromboembolism or more than one moderate risk factor for thromboe
G9842 - Patient has metastatic disease at diagnosis
G8947 - One or more neuropsychiatric symptoms
G9931 - Documentation of cha2ds2-vasc risk score of 0 or 1
G9902 - Patient screened for tobacco use and identified as a tobacco user
G8959 - Clinician treating major depressive disorder communicates to clinician treating comorbid condition
D0190 - Screening of a patient
H1000 - Prenatal care, at-risk assessment
G9918 - Functional status not performed, reason not otherwise specified
D9450 - CASE PRESENTATION

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
81443 - Genetic testing for severe inherited conditions (eg, cystic fibrosis, Ashkenazi Jewish-associated di
0060U - Twin zygosity, genomic targeted sequence analysis of chromosome 2, using circulating cell-free fetal
81221 - CFTR (cystic fibrosis transmembrane conductance regulator) (eg, cystic fibrosis) gene analysis; know
81470 - X-linked intellectual disability (XLID) (eg, syndromic and non-syndromic XLID); genomic sequence ana
81416 - Exome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis, each co
81432 - Hereditary breast cancer-related disorders (eg, hereditary breast cancer, hereditary ovarian cancer,
81415 - Exome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis
81435 - Hereditary colon cancer disorders (eg, Lynch syndrome, PTEN hamartoma syndrome, Cowden syndrome, fam