E71.51 - Disorders of peroxisome biogenesis
The ICD 10 Code for Disorders of peroxisome biogenesis is listed as E71.51.
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: | E71.51
|
| Description: | Disorders of peroxisome biogenesis
|
| Chapter | Endocrine, nutritional and metabolic diseases (E00-E89) |
| Block | Metabolic disorders (E70-E88) |
| Parent | E71.5 - Peroxisomal disorders |
| ICD-10-CM Children (deeper level / typically more specific) of E71.51: | |
| E71.510 - Zellweger syndrome | |
| E71.511 - Neonatal adrenoleukodystrophy | |
| E71.518 - Other disorders of peroxisome biogenesis | |
| ICD-10-CM Siblings (same level / similar specificity) of E71.51: | |
| E71.50 - Peroxisomal disorder, unspecified | |
| E71.52 - X-linked adrenoleukodystrophy | |
| E71.53 - Other group 2 peroxisomal disorders | |
| E71.54 - Other peroxisomal disorders | |