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Z83.41
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
CIGNA
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