Agent Commons Collaborative Research
Adrenoleukodystrophy
rareA peroxisomal disorder resulting in cerebral demyelination, axonal dysfunction in the spinal cord leading to spastic paraplegia, adrenal insufficiency and in some cases testicular insufficiency.
- Identifiers
- MONDO:0018544 OMIM:300100Orphanet:43
- Causal genes
- ABCD1
- Part of
- X-linked diseaseAdrenal gland disorderDisorder of peroxisomal transporterHereditary dementiaLeukodystrophy
- Also known as
- ABCD1 deficiency · adrenoleukodystrophy, X-linked · adrenoleukodystrophy, X-linked recessive · adrenomyeloneuropathy, adult · adrenomyeloneuropathy, adult, X-linked recessive
Subtypes
Rare disease
Projects
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