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Disease Information for Zellweger Cerebrhepatorenal syndrome: Disease Mechanism & Classification

Class: CLASS/Pediatric disorders (ex)
: CLASS/Liver/gallbladder/ducts (category)
: CLASS/Neurologic (category)
: CLASS/Urologic (category)
Pathophysiology: Pathophysiology/Gene locus 12p13.3; Pathophysiology/Gene locus 1p36.2; Pathophysiology/Gene locus 1q22; Pathophysiology/Gene locus 22q11.21; Pathophysiology/Gene locus 2p15; Pathophysiology/Gene locus 6q23-q24; Pathophysiology/Gene locus 7q21-q22; Pathophysiology/Gene locus Chromosome 1; Pathophysiology/Gene locus chromosome 12; Pathophysiology/Gene locus Chromosome 2; Pathophysiology/Gene locus chromosome 22; Pathophysiology/Gene locus Chromosome 22q; Pathophysiology/Gene locus Chromosome 6; Pathophysiology/Gene locus Chromosome 7; Pathophysiology/Gene Locus Identified/OMIM database; Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
: Pathophysiology/Defective myelin development
: Pathophysiology/Accumulation of wastes in cell/VLCFA; Pathophysiology/Peroxisomic Leukodystrophy; Pathophysiology/Scavenger protein defects
: Pathophysiology/Perioxisome defect brain, kidney,liver; Pathophysiology/Very long Chain fatty acid beta Oxidase failure
Process: PROCESS/Autosomal recessive disorder (ex); PROCESS/Congenital/developmental (category); PROCESS/Hereditofamilial (category); PROCESS/INCIDENCE/Rare disease (ex)
: PROCESS/Anomalies/Deformities/Malformations (EX)
: PROCESS/Leukodystrophy process (ex); PROCESS/Myelin involvement/disorder (ex)

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