| E72.53 |
Primary hyperoxaluria |
Notes ↗
|
| E72.530 |
Primary hyperoxaluria, type 1 |
Notes ↗
|
| E72.538 |
Other specified primary hyperoxaluria |
Notes ↗
|
| E72.539 |
Primary hyperoxaluria, unspecified |
Notes ↗
|
| E74.00 |
Glycogen storage disease, unspecified |
Notes ↗
|
| E74.01 |
von Gierke disease |
Notes ↗
|
| E74.03 |
Cori disease |
Notes ↗
|
| E74.04 |
McArdle disease |
Notes ↗
|
| E74.05 |
Lysosome-associated membrane protein 2 [LAMP2] deficiency |
Notes ↗
|
| E74.09 |
Other glycogen storage disease |
Notes ↗
|
| E79.1 |
Lesch-Nyhan syndrome |
Notes ↗
|
| E80.0 |
Hereditary erythropoietic porphyria |
Notes ↗
|
| E80.1 |
Porphyria cutanea tarda |
Notes ↗
|
| E80.20 |
Unspecified porphyria |
Notes ↗
|
| E80.21 |
Acute intermittent (hepatic) porphyria |
Notes ↗
|
| E80.29 |
Other porphyria |
Notes ↗
|
| E80.3 |
Defects of catalase and peroxidase |
Notes ↗
|
| E83.00 |
Disorder of copper metabolism, unspecified |
Notes ↗
|
| E83.01 |
Wilson's disease |
Notes ↗
|
| E83.09 |
Other disorders of copper metabolism |
Notes ↗
|
| E83.31 |
Familial hypophosphatemia |
Notes ↗
|
| E85.0 |
Non-neuropathic heredofamilial amyloidosis |
Notes ↗
|
| E85.1 |
Neuropathic heredofamilial amyloidosis |
Notes ↗
|
| E85.2 |
Heredofamilial amyloidosis, unspecified |
Notes ↗
|
| E85.3 |
Secondary systemic amyloidosis |
Notes ↗
|
| E85.4 |
Organ-limited amyloidosis |
Notes ↗
|
| E85.81 |
Light chain (AL) amyloidosis |
Notes ↗
|
| E85.82 |
Wild-type transthyretin-related (ATTR) amyloidosis |
Notes ↗
|
| E85.89 |
Other amyloidosis |
Notes ↗
|
| E85.9 |
Amyloidosis, unspecified |
Notes ↗
|
| E88.01 |
Alpha-1-antitrypsin deficiency |
Notes ↗
|
| E88.89 |
Other specified metabolic disorders |
Notes ↗
|