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Family history of multiple endocrine neoplasia [MEN] syndrome

ICD10CM code

Medical Policies and Guidelines for Family history of multiple endocrine neoplasia [MEN] syndrome

Related policies from health plans

Head and Neck Ultrasound - (0549)

Similar Codes


ICD10CM codes

Z83.41 - Family history of multiple endocrine neoplasia [MEN] syndrome
Z15.81 - Genetic susceptibility to multiple endocrine neoplasia [MEN]
E31.2 - Multiple endocrine neoplasia [MEN] syndromes
E31.20 - Multiple endocrine neoplasia [MEN] syndrome, unspecified
E31.23 - Multiple endocrine neoplasia [MEN] type IIB
E31.21 - Multiple endocrine neoplasia [MEN] type I
E31.22 - Multiple endocrine neoplasia [MEN] type IIA
Z83.4 - Family history of other endocrine, nutritional and metabolic diseases
Z83.49 - Family history of other endocrine, nutritional and metabolic diseases
Z85.85 - Personal history of malignant neoplasm of endocrine glands

HCPCS codes

G9555 - Documentation of medical reason(s) for recommending follow up imaging (e.g., patient has multiple en
G9842 - Patient has metastatic disease at diagnosis
G9097 - Oncology; disease status; esophageal cancer, limited to adenocarcinoma or squamous cell carcinoma as
G9552 - Incidental thyroid nodule < 1.0 cm noted in report
G8947 - One or more neuropsychiatric symptoms
G8721 - Pt category (primary tumor), pn category (regional lymph nodes), and histologic grade were documente
G8875 - Clinician diagnosed breast cancer preoperatively by a minimally invasive biopsy method
S3854 - Gene expression profiling panel for use in the management of breast cancer treatment
S3650 - Saliva test, hormone level; during menopause
G9549 - Documentation of medical reason(s) that follow-up imaging is indicated (e.g., patient has lymphadeno

CPT4 codes

81437 - Hereditary neuroendocrine tumor disorders (eg, medullary thyroid carcinoma, parathyroid carcinoma, m
60699 - Unlisted procedure, endocrine system
81322 - PTEN (phosphatase and tensin homolog) (eg, Cowden syndrome, PTEN hamartoma tumor syndrome) gene anal
81433 - Hereditary breast cancer-related disorders (eg, hereditary breast cancer, hereditary ovarian cancer,
81432 - 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
82941 - Gastrin
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
81321 - PTEN (phosphatase and tensin homolog) (eg, Cowden syndrome, PTEN hamartoma tumor syndrome) gene anal