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Z31.440
Encounter of male for testing for genetic disease carrier status for procreative management
ICD10CM code
Medical Policies and Guidelines for Encounter of male for testing for genetic disease carrier status for procreative management
Related policies from health plans
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Genetic Testing for TP53 Mutations
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Similar Codes
ICD10CM codes
Z31.440
- Encounter of male for testing for genetic disease carrier status for procreative management
Z31.430
- Encounter of female for testing for genetic disease carrier status for procreative management
Z31.44
- Encounter for genetic testing of male for procreative management
Z31.448
- Encounter for other genetic testing of male for procreative management
Z31.43
- Encounter for genetic testing of female for procreative management
Z31.438
- Encounter for other genetic testing of female for procreative management
Z13.71
- Encounter for nonprocreative screening for genetic disease carrier status
Z31.5
- Encounter for procreative genetic counseling
Z31.4
- Encounter for procreative investigation and testing
Z71.83
- Encounter for nonprocreative genetic counseling
HCPCS codes
H1000
- Prenatal care, at-risk assessment
D0190
- Screening of a patient
S0265
- Genetic counseling, under physician supervision, each 15 minutes
G0102
- Prostate cancer screening; digital rectal examination
T1023
- Screening to determine the appropriateness of consideration of an individual for participation in a
S3854
- Gene expression profiling panel for use in the management of breast cancer treatment
J3399
- Injection, onasemnogene abeparvovec-xioi, per treatment, up to 5x10^15 vector genomes
G9228
- Chlamydia, gonorrhea and syphilis screening results documented (report when results are present for
D1110
- PROPHYLAXIS-ADULT
G9618
- Documentation of screening for uterine malignancy or those that had an ultrasound and/or endometrial
CPT4 codes
81425
- Genome (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
96040
- Medical genetics and genetic counseling services, each 30 minutes face-to-face with patient/family
81422
- Fetal chromosomal microdeletion(s) genomic sequence analysis (eg, DiGeorge syndrome, Cri-du-chat syn
00924
- Anesthesia for procedures on male genitalia (including open urethral procedures); undescended testis
4293F
- Patient screened for high-risk sexual behavior (HIV)
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
89261
- Sperm isolation; complex prep (eg, Percoll gradient, albumin gradient) for insemination or diagnosis
81507
- Fetal aneuploidy (trisomy 21, 18, and 13) DNA sequence analysis of selected regions using maternal p
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