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ICD-10-CM E83.82 — Disorders of pyrophosphate met… | Codelle

ICD-10-CM/E83.8/E83.82

E83.82

ICD-10-CM

Disorders of pyrophosphate metabolism

Code Hierarchy

▲E83.8Other disorders of mineral metabolism

E83.82(current)

Subcodes (6)

E83.820Gen arterial calcifcn of infancy with unsp genetic causality

E83.821ENPP1 deficiency causing gen arterial calcifcn of infancy

E83.822ENPP1 def cause autosom recess hypophosphate rickets type 2

E83.823ABCC6 deficiency causing gen arterial calcifcn of infancy

E83.824ABCC6 deficiency causing pseudoxanthoma elasticum

E83.825CD73 deficiency causing arterial calcification

Same Category

E83Disorders of mineral metabolism E83.0Disorders of copper metabolism E83.00Disorder of copper metabolism, unspecified E83.01Wilson's disease E83.09Other disorders of copper metabolism E83.1Disorders of iron metabolism E83.10Disorder of iron metabolism, unspecified E83.11Hemochromatosis E83.110Hereditary hemochromatosis E83.111Hemochromatosis due to repeated red blood cell transfusions

+5 more in this category