E00–E89: Endocrine, Nutritional and Metabolic Diseases
Chapter 4 of ICD-10-CM 2027, 1,270 codes in 10 blocks.
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Chapter instructions
Excludes1: not coded here, use a different code
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)
Codes in this chapter
All codesBillable only1,270 results
- E83.19Other disorders of iron metabolism
- E83.2Disorders of zinc metabolism
- E83.3Disorders of phosphorus metabolism and phosphatases
- E83.30Disorder of phosphorus metabolism, unspecified
- E83.31Familial hypophosphatemia
- E83.32Hereditary vitamin D-dependent rickets (type 1) (type 2)
- E83.39Other disorders of phosphorus metabolism
- E83.4Disorders of magnesium metabolism
- E83.40Disorders of magnesium metabolism, unspecified
- E83.41Hypermagnesemia
- E83.42Hypomagnesemia
- E83.49Other disorders of magnesium metabolism
- E83.5Disorders of calcium metabolism
- E83.50Unspecified disorder of calcium metabolism
- E83.51Hypocalcemia
- E83.52Hypercalcemia
- E83.59Other disorders of calcium metabolism
- E83.8Other disorders of mineral metabolism
- E83.81Hungry bone syndrome
- E83.82Disorders of pyrophosphate metabolism
- E83.820Generalized arterial calcification of infancy with unspecified genetic causality
- E83.821ENPP1 deficiency causing generalized arterial calcification of infancy
- E83.822ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2
- E83.823ABCC6 deficiency causing generalized arterial calcification of infancy
- E83.824ABCC6 deficiency causing pseudoxanthoma elasticum
- E83.825CD73 deficiency causing arterial calcification
- E83.89Other disorders of mineral metabolism
- E83.9Disorder of mineral metabolism, unspecified
- E84Cystic fibrosis
- E84.0Cystic fibrosis with pulmonary manifestations
- E84.1Cystic fibrosis with intestinal manifestations
- E84.11Meconium ileus in cystic fibrosis
- E84.19Cystic fibrosis with other intestinal manifestations
- E84.8Cystic fibrosis with other manifestations
- E84.9Cystic fibrosis, unspecified
- E85Amyloidosis
- E85.0Non-neuropathic heredofamilial amyloidosis
- E85.1Neuropathic heredofamilial amyloidosis
- E85.2Heredofamilial amyloidosis, unspecified
- E85.3Secondary systemic amyloidosis
- E85.4Organ-limited amyloidosis
- E85.8Other amyloidosis
- E85.81Light chain (AL) amyloidosis
- E85.82Wild-type transthyretin-related (ATTR) amyloidosis
- E85.89Other amyloidosis
- E85.9Amyloidosis, unspecified
- E86Volume depletion
- E86.0Dehydration
- E86.1Hypovolemia
- E86.9Volume depletion, unspecified