5C57 Peroxisomal diseases
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
Peroxisomal disorders represent a class of medical conditions caused by defects in peroxisome functions. This may be due to defects in single enzymes important for peroxisome function or in peroxins, proteins encoded by PEX genes that are critical for normal peroxisome assembly and biogenesis.
code elsewhere
- Primary hyperoxaluria type 1 (5C51.20)
- Adrenoleukodystrophy (8A44.1)
- Rhizomelic chondrodysplasia punctata (LD24.04)
- Glutaric aciduria type 3 (5C50.E0)
sections/codes in this section (5C57-5C57)
- Disorders of peroxisome biogenesis (5C57.0)
- Disorders of peroxisomal alpha-, beta- or omega-oxidation (5C57.1)
- Other specified peroxisomal diseases (5C57.Y)
- Peroxisomal diseases, unspecified (5C57.Z)
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