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Genetic susceptibility to multiple endocrine neoplasia [MEN]

ICD10CM code

Similar Codes


ICD10CM codes

Z15.81 - Genetic susceptibility to multiple endocrine neoplasia [MEN]
Z83.41 - Family history of multiple endocrine neoplasia [MEN] syndrome
E31.21 - Multiple endocrine neoplasia [MEN] type I
E31.23 - Multiple endocrine neoplasia [MEN] type IIB
E31.20 - Multiple endocrine neoplasia [MEN] syndrome, unspecified
E31.22 - Multiple endocrine neoplasia [MEN] type IIA
E31.2 - Multiple endocrine neoplasia [MEN] syndromes
Z15.0 - Genetic susceptibility to malignant neoplasm
Z15.04 - Genetic susceptibility to malignant neoplasm of endometrium
Z15.03 - Genetic susceptibility to malignant neoplasm of prostate

HCPCS codes

G9555 - Documentation of medical reason(s) for recommending follow up imaging (e.g., patient has multiple en
G9097 - Oncology; disease status; esophageal cancer, limited to adenocarcinoma or squamous cell carcinoma as
G9842 - Patient has metastatic disease at diagnosis
G8947 - One or more neuropsychiatric symptoms
S3854 - Gene expression profiling panel for use in the management of breast cancer treatment
G9552 - Incidental thyroid nodule < 1.0 cm noted in report
G8875 - Clinician diagnosed breast cancer preoperatively by a minimally invasive biopsy method
G8972 - One or more high risk factors for thromboembolism or more than one moderate risk factor for thromboe
G0105 - Colorectal cancer screening; colonoscopy on individual at high risk
G0101 - Cervical or vaginal cancer screening; pelvic and clinical breast examination

CPT4 codes

81437 - Hereditary neuroendocrine tumor disorders (eg, medullary thyroid carcinoma, parathyroid carcinoma, m
60699 - Unlisted procedure, endocrine system
81432 - Hereditary breast cancer-related disorders (eg, hereditary breast cancer, hereditary ovarian cancer,
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
81322 - PTEN (phosphatase and tensin homolog) (eg, Cowden syndrome, PTEN hamartoma tumor syndrome) gene anal
81321 - PTEN (phosphatase and tensin homolog) (eg, Cowden syndrome, PTEN hamartoma tumor syndrome) gene anal
81500 - Oncology (ovarian), biochemical assays of two proteins (CA-125 and HE4), utilizing serum, with menop
81436 - Hereditary colon cancer disorders (eg, Lynch syndrome, PTEN hamartoma syndrome, Cowden syndrome, fam
82941 - Gastrin