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Encounter of female for testing for genetic disease carrier status for procreative management

ICD10CM code

Medical Policies and Guidelines for Encounter of female for testing for genetic disease carrier status for procreative management

Related policies from health plans

Genetic Testing for Inherited Diseases
Genetic Testing for Inherited Diseases
Genetic Testing for Inherited Diseases
Genetic Testing for Inherited Diseases
Genetic Testing for TP53 Mutations
Genetic Testing for Reproductive Carrier Screening and Prenatal Diagnosis - (0514)
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-13 Genetic Testing for Inherited Diseases
CG-GENE-18 Genetic Testing for TP53 Mutations

Similar Codes


ICD10CM codes

Z31.430 - Encounter of female for testing for genetic disease carrier status for procreative management
Z31.440 - Encounter of male for testing for genetic disease carrier status 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
Z31.44 - Encounter for genetic testing of male for procreative management
Z31.448 - Encounter for other genetic testing of male for procreative management
Z13.71 - Encounter for nonprocreative screening for genetic disease carrier status
Z31.5 - Encounter for procreative genetic counseling
Z31.7 - Encounter for procreative management and counseling for gestational carrier
Z31.41 - Encounter for fertility testing

HCPCS codes

H1000 - Prenatal care, at-risk assessment
D0190 - Screening of a patient
G9618 - Documentation of screening for uterine malignancy or those that had an ultrasound and/or endometrial
S3854 - Gene expression profiling panel for use in the management of breast cancer treatment
G0101 - Cervical or vaginal cancer screening; pelvic and clinical breast examination
T1023 - Screening to determine the appropriateness of consideration of an individual for participation in a
S0265 - Genetic counseling, under physician supervision, each 15 minutes
J3399 - Injection, onasemnogene abeparvovec-xioi, per treatment, up to 5x10^15 vector genomes
S4981 - Insertion of levonorgestrel-releasing intrauterine system
S4989 - Contraceptive intrauterine device (e.g., progestacert iud), including implants and supplies

CPT4 codes

0060U - Twin zygosity, genomic targeted sequence analysis of chromosome 2, using circulating cell-free fetal
81425 - Genome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis
96040 - Medical genetics and genetic counseling services, each 30 minutes face-to-face with patient/family
81432 - Hereditary breast cancer-related disorders (eg, hereditary breast cancer, hereditary ovarian cancer,
81422 - Fetal chromosomal microdeletion(s) genomic sequence analysis (eg, DiGeorge syndrome, Cri-du-chat syn
81507 - Fetal aneuploidy (trisomy 21, 18, and 13) DNA sequence analysis of selected regions using maternal p
81433 - Hereditary breast cancer-related disorders (eg, hereditary breast cancer, hereditary ovarian cancer,
81512 - Fetal congenital abnormalities, biochemical assays of five analytes (AFP, uE3, total hCG, hyperglyco
81508 - Fetal congenital abnormalities, biochemical assays of two proteins (PAPP-A, hCG [any form]), utilizi
4293F - Patient screened for high-risk sexual behavior (HIV)