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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