Chapter 4 – Endocrine, Nutritional & Metabolic Diseases
23 New Codes
Hyperoxaluria
E11.A Type 2 diabetes mellitus w/out complications in remission
E72.53 Primary hyperoxaluria
- E78.530 Primary hyperoxaluria, type 1
- E72.538 Other specified primary hyperoxaluria
- E72.539 Primary hyperoxaluria, unspecified
- E72.540 Dietary hyperoxaluria
- E72.541 Enteric hyperoxaluria
- E72.548 Other secondary hyperoxaluria
- E72.549 Secondary hyperoxaluria, unspecified
Hypercholesterolemia
- E78.01 Familial hypercholesterolemia
- E78.010 Homozygous familial hypercholesterolemia [HoFH]
- E78.011 Heterozygous familial hypercholesterolemia [HeFH]
- E78.019 Familial hypercholesterolemia, unspecified
Deficiency
- E83.820 Generalized arterial calcification of infancy with unspecified genetic causality
- E83.821 ENPP1 deficiency causing generalized arterial calcification of infancy
- E83.822 ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2
- E83.823 ABCC6 deficiency causing generalized arterial calcification of infancy
- E83.824 ABCC6 deficiency causing pseudoxanthomas elasticum
- E83.825 CD73 deficiency causing arterial calcification
Code also – need additional codes if applicable
Lipodystrophy
E88.1 Lipodystrophy, not elsewhere classified
- E88.10 Lipodystrophy, unspecified
- E88.11 Partial lipodystrophy
- E88.12 Generalized lipodystrophy
- E88.13 Localized lipodystrophy
- E88.14 HIV-associate lipodystrophy
- E88.19 Other lipodystrophy not elsewhere classified

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