E80.0 - Hereditary erythropoietic porphyria
The ICD 10 Code for Hereditary erythropoietic porphyria is listed as E80.0.
Additional information concerning this code and description can be found below including ICD 9 crosswalks / GEMS, chapter information, and DRGs where available.
| ICD 10 CM Field | Value |
|---|---|
| Diagnosis Code: | E80.0
|
| Description: | Hereditary erythropoietic porphyria
|
| Diagnostic Related Groups
(MS-DRG v30.0) |
642 - Inborn And Other Disorders Of Metabolism
|
| Chapter | Endocrine, nutritional and metabolic diseases (E00-E89) |
| Block | Metabolic disorders (E70-E88) |
| Parent | E80 - Disorders of porphyrin and bilirubin metabolism |
| ICD-9-CM Diagnosis Codes General Equivalence Mappings (GEMS): | |
| ICD 9 Dx Code: | 277.1 - Disorders of porphyrin metabolism (approximate) |
| ICD-10-CM Siblings (same level / similar specificity) of E80.0: | |
| E80.1 - Porphyria cutanea tarda | |
| E80.2 - Other and unspecified porphyria | |
| E80.3 - Defects of catalase and peroxidase | |
| E80.4 - Gilbert syndrome | |
| E80.5 - Crigler-Najjar syndrome | |
| E80.6 - Other disorders of bilirubin metabolism | |
| E80.7 - Disorder of bilirubin metabolism, unspecified | |