Medical condition
| Neonatal adrenoleukodystrophy |
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| Other names | NALD[1] |
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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.[2]
References
- ^ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Neonatal adrenoleukodystrophy". www.orpha.net. Retrieved 17 March 2019.
{{cite web}}: CS1 maint: numeric names: authors list (link) - ^ "#202370 Adrenoleukodystrophy, Autosomal Neonatal Form". Johns Hopkins University. Retrieved 2012-06-24.
External links
| Classification | D - ICD-10: E71.3
- ICD-10-CM: E71.511
- OMIM: 202370 266510 601539 614863 614867 614871 614873
- MeSH: D018901
- SNOMED CT: 238061001
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| External resources | |
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Genetic disorder, organelle: Peroxisomal disorders and lysosomal structural disorders |
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| Peroxisome biogenesis disorder | - Zellweger syndrome
- Neonatal adrenoleukodystrophy
- Infantile Refsum disease
- Adult Refsum disease-2
- RCP 1
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| Enzyme-related | |
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| Transporter-related | |
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| Lysosomal | |
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See also: proteins, intermediates |
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