 E83 |
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Disorders of mineral metabolism  |
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| Excludes1 |
dietary mineral deficiency (E58-E61)
parathyroid disorders (E20-E21)
vitamin D deficiency (E55.-)
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| E83.0 |
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Disorders of copper metabolism |
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 E83.00 |
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Disorder of copper metabolism, unspecified |
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| E83.01 |
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Wilson's disease |
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| CodeAlso |
associated Kayser Fleischer ring (H18.04-)
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| | |
| E83.09 |
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Other disorders of copper metabolism |
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| Menkes' (kinky hair) (steely hair) disease |
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| |
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| E83.1 |
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Disorders of iron metabolism |
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| E83.10 |
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Disorder of iron metabolism, unspecified |
| | |
| E83.11 |
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Hemochromatosis |
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| Excludes1 |
GALD (P78.84)
Gestational alloimmune liver disease (P78.84)
Neonatal hemochromatosis (P78.84)
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|
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| E83.110 |
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Hereditary hemochromatosis |
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| Bronzed diabetes | | Pigmentary cirrhosis (of liver) | | Primary (hereditary) hemochromatosis |
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| | |
| E83.111 |
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Hemochromatosis due to repeated red blood cell transfusions |
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| Iron overload due to repeated red blood cell transfusions | | Transfusion (red blood cell) associated hemochromatosis |
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| | |
| E83.118 |
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Other hemochromatosis |
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| E83.119 |
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Hemochromatosis, unspecified |
| | | |
| E83.19 |
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Other disorders of iron metabolism |
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| UseAdditionalCode |
code, if applicable, for idiopathic pulmonary hemosiderosis (J84.03)
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| E83.2 |
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Disorders of zinc metabolism |
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| Acrodermatitis enteropathica |
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| E83.3 |
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Disorders of phosphorus metabolism and phosphatases |
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| Excludes1 |
adult osteomalacia (M83.-)
osteoporosis (M80.-)
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| Excludes2 |
disorders of pyrophosphate metabolism (E83.82-)
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|
| |
| E83.30 |
|
Disorder of phosphorus metabolism, unspecified |
| | |
| E83.31 |
|
Familial hypophosphatemia |
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| Vitamin D-resistant osteomalacia | | Vitamin D-resistant rickets |
| Excludes1 |
vitamin D-deficiency rickets (E55.0)
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| | |
| E83.32 |
|
Hereditary vitamin D-dependent rickets (type 1) (type 2) |
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| 25-hydroxyvitamin D 1-alpha-hydroxylase deficiency | | Pseudovitamin D deficiency | | Vitamin D receptor defect |
|
| | |
| E83.39 |
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Other disorders of phosphorus metabolism |
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| Acid phosphatase deficiency | | Hypophosphatasia |
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| |
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| E83.4 |
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Disorders of magnesium metabolism |
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| E83.40 |
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Disorders of magnesium metabolism, unspecified |
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| E83.41 |
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Hypermagnesemia |
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| E83.42 |
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Hypomagnesemia |
| | |
| E83.49 |
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Other disorders of magnesium metabolism |
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| E83.5 |
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Disorders of calcium metabolism |
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| Excludes1 |
autoimmune hypoparathyroidism (E20.812)
autosomal dominant hypocalcemia (E20.810)
chondrocalcinosis (M11.1-M11.2)
hungry bone syndrome (E83.81)
hyperparathyroidism (E21.0-E21.3)
secondary hypoparathyroidism in diseases classified elsewhere (E20.811)
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|
| |
| E83.50 |
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Unspecified disorder of calcium metabolism |
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| E83.51 |
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Hypocalcemia |
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| E83.52 |
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Hypercalcemia |
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| Familial hypocalciuric hypercalcemia |
|
| | |
| E83.59 |
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Other disorders of calcium metabolism |
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| E83.8 |
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Other disorders of mineral metabolism |
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| E83.81 |
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Hungry bone syndrome |
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| E83.82 |
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Disorders of pyrophosphate metabolism |
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| E83.820 |
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Generalized arterial calcification of infancy with unspecified genetic causality |
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| CodeAlso |
, if applicable, associated conditions such as:
heart failure (I50.-)
other secondary hypertension (I15.8)
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|
| | |
| E83.821 |
|
ENPP1 deficiency causing generalized arterial calcification of infancy |
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| CodeAlso |
, if applicable, associated conditions such as:
heart failure (I50.-)
other secondary hypertension (I15.8)
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|
| | |
| E83.822 |
|
ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2 |
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| E83.823 |
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ABCC6 deficiency causing generalized arterial calcification of infancy |
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| CodeAlso |
, if applicable, associated conditions such as:
heart failure (I50.-)
other secondary hypertension (I15.8)
|
|
| | |
| E83.824 |
|
ABCC6 deficiency causing pseudoxanthoma elasticum |
| | |
| E83.825 |
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CD73 deficiency causing arterial calcification |
| | | |
| E83.89 |
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Other disorders of mineral metabolism |
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| E83.9 |
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Disorder of mineral metabolism, unspecified |
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