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Search all medical codes
Z83.4
Family history of other endocrine, nutritional and metabolic diseases
ICD10CM code
Similar Codes
ICD10CM codes
Z83.4
- Family history of other endocrine, nutritional and metabolic diseases
Z83.49
- Family history of other endocrine, nutritional and metabolic diseases
Z86.39
- Personal history of other endocrine, nutritional and metabolic disease
Z86.3
- Personal history of endocrine, nutritional and metabolic diseases
Z83.3
- Family history of diabetes mellitus
Z84.8
- Family history of other specified conditions
Z83
- Family history of other specific disorders
Z84.89
- Family history of other specified conditions
Z83.43
- Family history of other disorder of lipoprotein metabolism and other lipidemias
Z83.79
- Family history of other diseases of the digestive system
HCPCS codes
S9435
- Medical foods for inborn errors of metabolism
G9842
- Patient has metastatic disease at diagnosis
G9555
- Documentation of medical reason(s) for recommending follow up imaging (e.g., patient has multiple en
G8726
- Clinician has documented reason for not performing fasting lipid profile (e.g., patient declined, ot
G8494
- All quality actions for the applicable measures in the diabetes mellitus (dm) measures group have be
B4157
- Enteral formula, nutritionally complete, for special metabolic needs for inherited disease of metabo
G8485
- I intend to report the diabetes mellitus (dm) measures group
G8947
- One or more neuropsychiatric symptoms
B4154
- Enteral formula, nutritionally complete, for special metabolic needs, excludes inherited disease of
S9465
- Diabetic management program, dietitian visit
CPT4 codes
60699
- Unlisted procedure, endocrine system
81437
- Hereditary neuroendocrine tumor disorders (eg, medullary thyroid carcinoma, parathyroid carcinoma, m
84235
- Receptor assay; endocrine, other than estrogen or progesterone (specify hormone)
81425
- Genome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis
81412
- Ashkenazi Jewish associated disorders (eg, Bloom syndrome, Canavan disease, cystic fibrosis, familia
82941
- Gastrin
5010F
- Findings of dilated macular or fundus exam communicated to the physician or other qualified health c
81416
- Exome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis, each co
43848
- Revision, open, of gastric restrictive procedure for morbid obesity, other than adjustable gastric r
84681
- C-peptide
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