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Genetic susceptibility to other malignant neoplasm

ICD10CM code

Medical Policies and Guidelines for Genetic susceptibility to other malignant neoplasm

Related policies from health plans

Jemperli (dostarlimab)
Colorectal Cancer Screening (CG024)
Wireless Capsule Endoscopy for Gastrointestinal Imaging and the Patency Capsule
CG-MED-70 Wireless Capsule Endoscopy for Gastrointestinal Imaging and the Patency Capsule

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