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Z15.09
Genetic susceptibility to other malignant neoplasm
ICD10CM code
Medical Policies and Guidelines for Genetic susceptibility to other malignant neoplasm
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Similar Codes
ICD10CM codes
Z15.09
- Genetic susceptibility to other malignant neoplasm
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
Z15.89
- Genetic susceptibility to other disease
Z15.8
- Genetic susceptibility to other disease
Z15.02
- Genetic susceptibility to malignant neoplasm of ovary
Z15.04
- Genetic susceptibility to malignant neoplasm of endometrium
Z15
- Genetic susceptibility to disease
Z80.9
- Family history of malignant neoplasm, unspecified
HCPCS codes
G9420
- Specimen site other than anatomic location of lung or is not classified as primary non-small cell lu
G9097
- Oncology; disease status; esophageal cancer, limited to adenocarcinoma or squamous cell carcinoma as
G9842
- Patient has metastatic disease at diagnosis
G0105
- Colorectal cancer screening; colonoscopy on individual at high risk
D7430
- Excision of benign tumor-lesion diameter up to 1.25 cm
J9999
- Not otherwise classified, antineoplastic drugs
G9552
- Incidental thyroid nodule < 1.0 cm noted in report
G9555
- Documentation of medical reason(s) for recommending follow up imaging (e.g., patient has multiple en
G9754
- A finding of an incidental pulmonary nodule
G8875
- Clinician diagnosed breast cancer preoperatively by a minimally invasive biopsy method
CPT4 codes
88239
- Tissue culture for neoplastic disorders; solid tumor
81432
- Hereditary breast cancer-related disorders (eg, hereditary breast cancer, hereditary ovarian cancer,
81437
- Hereditary neuroendocrine tumor disorders (eg, medullary thyroid carcinoma, parathyroid carcinoma, m
81433
- Hereditary breast cancer-related disorders (eg, hereditary breast cancer, hereditary ovarian cancer,
81435
- Hereditary colon cancer disorders (eg, Lynch syndrome, PTEN hamartoma syndrome, Cowden syndrome, fam
43611
- Excision, local; malignant tumor of stomach
81263
- IGH@ (Immunoglobulin heavy chain locus) (eg, leukemia and lymphoma, B-cell), variable region somatic
3775F
- Adenoma(s) or other neoplasm detected during screening colonoscopy (SCADR)
0080U
- Oncology (lung), mass spectrometric analysis of galectin-3-binding protein and scavenger receptor cy
81277
- Cytogenomic neoplasia (genome-wide) microarray analysis, interrogation of genomic regions for copy n