Disease Information for Schilder disease/Adrenoleukodystrophy: Disease Mechanism & Classification

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Class
CLASS/Pediatric disorders (ex)
CLASS/Adrenal gland disorders (ex).
CLASS/Brain/CNS disorder (ex)
CLASS/Cerebral cortex disorder (ex)
CLASS/Neurologic (category)
Pathophysiology
Pathophysiology/Adult variant disease milder
Pathophysiology/Gene locus 12p13.3
Pathophysiology/Gene locus 22q11.21
Pathophysiology/Gene locus 2p15
Pathophysiology/Gene locus 7q21-q22
Pathophysiology/Gene locus Chromosome 1
Pathophysiology/Gene locus Chromosome 22q
Pathophysiology/Gene locus Chromosome X.
Pathophysiology/Gene Locus Identified/OMIM database
Pathophysiology/Gene locus Xq28
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Hereditary variance/ X-linked not always
Pathophysiology/Single gene locus indentified
Pathophysiology/Adrenal destruction/atrophy/infiltrate
Pathophysiology/Cerebral demyelination
Pathophysiology/Cortical motor neuron disease
Pathophysiology/Demyelination
Pathophysiology/Peroxisomic Leukodystrophy
Process
PROCESS/Eponymic (category)
PROCESS/Hereditary dominance/incomplete penetrance (ex).
PROCESS/Hereditofamilial (category)
PROCESS/INCIDENCE/Rare disease (ex)
PROCESS/Sex-linked (X-linked) recessive inheritance (ex)
PROCESS/Use/Age/atrophic disorder (category)
PROCESS/Variant expressions/Subsets (ex)
PROCESS/CNS/White matter disorder (ex)
PROCESS/Leukodystrophy process (ex)
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