Neonatal adrenoleukodystrophy

For the X-linked, juvenile or adult-onset condition, see Adrenoleukodystrophy. Medical condition

Neonatal adrenoleukodystrophy
Other names	NALD

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.

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.

Classification	D ICD-10: E71.3 ICD-10-CM: E71.511 OMIM: 202370 266510 601539 614863 614867 614871 614873 MeSH: D018901 SNOMED CT: 238061001
External resources	Orphanet: 44

v t e Genetic disorder, organelle: Peroxisomal disorders and lysosomal structural disorders
Peroxisome biogenesis disorder	Zellweger syndrome Neonatal adrenoleukodystrophy Infantile Refsum disease Adult Refsum disease-2 RCP 1
Enzyme-related	Acatalasia RCP 2&3 Mevalonate kinase deficiency D-bifunctional protein deficiency Adult Refsum disease-1
Transporter-related	X-linked adrenoleukodystrophy
Lysosomal	Danon disease
See also: proteins, intermediates

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