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Results 1 - 6 of 6 for Adrenomyeloneuropathy
  1. X-linked adrenoleukodystrophy 
    X-linked adrenoleukodystrophy is a genetic disorder that mainly affects the nervous system and the adrenal glands, which are located on ... There are four distinct types of X-linked adrenoleukodystrophy: a childhood cerebral form, an adrenomyeloneuropathy type, an ...
    https://medlineplus.gov/.../condition/x-linked-adrenoleukodystrophy - Genetics
  2. ABCD1 gene 
    The ABCD1 gene provides instructions for producing the adrenoleukodystrophy protein (ALDP). ALDP is located in the membranes ... gene have been found to cause X-linked adrenoleukodystrophy. This condition is characterized by varying degrees of ...
    https://medlineplus.gov/genetics/gene/abcd1 - Genetics
  3. Peroxisomal acyl-CoA oxidase deficiency 
    ... coenzyme A oxidase deficiency Pseudo-NALD Pseudoadrenoleukodystrophy Pseudoneonatal adrenoleukodystrophy Straight-chain acyl-CoA oxidase deficiency Genetic Testing ...
    https://medlineplus.gov/.../peroxisomal-acyl-coa-oxidase-deficiency - Genetics
  4. Zellweger spectrum disorder 
    ... as Zellweger syndrome, the intermediate form was neonatal adrenoleukodystrophy (NALD), and the mild form was infantile Refsum ...
    https://medlineplus.gov/.../condition/zellweger-spectrum-disorder - Genetics
  5. Autoimmune Addison disease 
    ... features of other genetic conditions, including X-linked adrenoleukodystrophy and autoimmune polyglandular syndrome, type 1, which are ...
    https://medlineplus.gov/.../condition/autoimmune-addison-disease - Genetics
  6. ACOX1 gene 
    ... response in acyl-CoA oxidase 1 deficiency (pseudoneonatal adrenoleukodystrophy). Endocrinology. 2012 Jun;153(6):2568-75. doi: ...
    https://medlineplus.gov/genetics/gene/acox1 - Genetics