Pick one of the followings
*Some genes may be words of complete meaning. In any case, if present, they are relevant key words.
Legend:
| *** | p-value <= 0.001 |
| ** | p-value <= 0.01 |
| * | p-value <= 0.05 |
| n.s. | not significant |
|
Top Ranked Genes, Molecules or Short Names*
|
Top Ranked Key Phrases
Long chain fatty acids vlcfa ***
 Cerebro hepato renal zellweger syndrome ***
X linked adrenoleukodystrophy x ald ***
Long chain fatty acids ***
Cerebro hepato renal syndrome ***
Rhizomelic chondrodysplasia punctata rcdp ***
Peroxisomal beta oxidation enzymes ***
Peroxisome biogenesis disorders pbds ***
Peroxisome biogenesis disorders pbd ***
Infantile refsum disease ird **
Dihydroxyacetone phosphate acyltransferase **
Rhizomelic chondrodysplasia punctata **
X linked adrenoleukodystrophy **
Peroxisomal beta oxidation **
Peroxisomal matrix proteins *
Generalized peroxisomal disorders *
Peroxisomal biogenesis disorders *
Peroxisome biogenesis disorders *
Infantile refsum disease *
Cultured skin fibroblasts *
Neonatal adrenoleukodystrophy nald *
Zellweger syndrome patients n.s.
|
Top Ranked Mesh Terms
Molecular sequence data ***
Genetic complementation test ***
Metabolism inborn errors ***
Peroxisomal disorders ***
Magnetic resonance imaging ***
Abnormalities multiple ***
Disease models animal ***
Receptors cytoplasmic and nuclear ***
Adenosine triphosphatases **
Gas chromatography-mass spectrometry **
Intracellular membranes **
Fluorescent antibody technique **
Dna mutational analysis **
Diffuse cerebral sclerosis of schilder **
Diagnosis differential **
Lipid metabolism inborn errors **
Atp-binding cassette transporters **
Sequence homology amino acid **
Chondrodysplasia punctata **
3-hydroxyacyl coa dehydrogenases **
Fatty acids unsaturated **
Acetyl-coa c-acetyltransferase *
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Top Ranked Mesh Terms (Symptoms)
Intellectual disability *
Hearing loss sensorineural *
Genetic predisposition to disease n.s.
Fetal growth retardation n.s.
Chromosome aberrations n.s.
Chromosome inversion n.s.
Agenesis of corpus callosum n.s.
Multiple organ failure n.s.
Cell transformation viral n.s.
Sex chromosome aberrations n.s.
Respiratory aspiration n.s.
Translocation genetic n.s.
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