Neonatal adrenoleukodystrophy
| Neonatal adrenoleukodystrophy | |
|---|---|
| Classification and external resources | |
| ICD-10 | E71.3 |
| OMIM | 202370 266510 601539 614863 614867 614871 614873 |
| MeSH | D018901 |
| Orphanet | 44 |
Neonatal adrenoleukodystrophy is an inborn error of peroxisome biogenesis. It is part of the Zellweger spectrum. It has been linked with multiple genes (at least five) associated with peroxisome biogenesis, and has an autosomal recessive pattern of inheritance.[1]
References
- ↑ "#202370 Adrenoleukodystrophy, Autosomal Neonatal Form". Johns Hopkins University. Retrieved 2012-06-24.
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