HCC 50 (V28)
Amyloidosis, Porphyria, and Other Specified Metabolic Disorders
32 ICD-10-CM codes map to this category in the CMS-HCC V28 risk adjustment model for payment year 2027. All 115 HCCs
| E72.53 | Primary hyperoxaluria |
| E72.530 | Primary hyperoxaluria, type 1 |
| E72.538 | Other specified primary hyperoxaluria |
| E72.539 | Primary hyperoxaluria, unspecified |
| E74.00 | Glycogen storage disease, unspecified |
| E74.01 | von Gierke disease |
| E74.03 | Cori disease |
| E74.04 | McArdle disease |
| E74.05 | Lysosome-associated membrane protein 2 [LAMP2] deficiency |
| E74.09 | Other glycogen storage disease |
| E79.1 | Lesch-Nyhan syndrome |
| E80.0 | Hereditary erythropoietic porphyria |
| E80.1 | Porphyria cutanea tarda |
| E80.20 | Unspecified porphyria |
| E80.21 | Acute intermittent (hepatic) porphyria |
| E80.29 | Other porphyria |
| E80.3 | Defects of catalase and peroxidase |
| E83.00 | Disorder of copper metabolism, unspecified |
| E83.01 | Wilson's disease |
| E83.09 | Other disorders of copper metabolism |
| E83.31 | Familial hypophosphatemia |
| E85.0 | Non-neuropathic heredofamilial amyloidosis |
| E85.1 | Neuropathic heredofamilial amyloidosis |
| E85.2 | Heredofamilial amyloidosis, unspecified |
| E85.3 | Secondary systemic amyloidosis |
| E85.4 | Organ-limited amyloidosis |
| E85.81 | Light chain (AL) amyloidosis |
| E85.82 | Wild-type transthyretin-related (ATTR) amyloidosis |
| E85.89 | Other amyloidosis |
| E85.9 | Amyloidosis, unspecified |
| E88.01 | Alpha-1-antitrypsin deficiency |
| E88.89 | Other specified metabolic disorders |