Biochemistry, Genetics and Molecular Biology
Adrenoleukodystrophy
55%
Alcohol Dehydrogenase
8%
Alcohol Oxidation
9%
Aldehyde Dehydrogenase
93%
Allele
9%
Alpha Oxidation
16%
Autosomal Recessive Disorder
16%
Autosomal Recessive Inheritance
9%
Beta Oxidation
14%
Biogenesis
17%
Biotin Deficiency
7%
Cetyl Alcohol
13%
Chromatin Structure
14%
Chromosome 17p
7%
Consanguinity
8%
Enzyme
14%
Enzyme Activity
16%
Ethanol Metabolism
17%
Exon
19%
Fatty Alcohol
76%
Fatty Aldehyde
100%
Fibroblast
45%
Genetic Disorder
9%
Genetics
45%
Genotyping
9%
Haplotype
16%
Intellectual Disability
22%
Keratinocyte
8%
Lectin
9%
Lipid
17%
Lipid Metabolism
16%
Magnetism
18%
Medical Decision Making
9%
Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency
7%
Metabolic Pathway
22%
Metabolite
8%
Metabolomics
14%
Missense Mutation
13%
Molecular Genetics
12%
Mouse
8%
Multiple Sulfatase Deficiency
14%
Newborn Screening
12%
Oxidoreductase
31%
Peroxisome
17%
Plasmalogen
17%
Saturated Fatty Acid
8%
Sjögren-Larsson Syndrome
40%
Splice Site Mutation
7%
Stearyl Alcohol
7%
Very Long Chain Fatty Acid
17%
Keyphrases
Adrenoleukodystrophy
24%
Adrenomyeloneuropathy
9%
Alcohol Metabolism
11%
Aldehydes
9%
ALDH3A2
18%
ALDH3A2 Gene
14%
Aliphatic Alcohols
7%
Aliphatic Aldehydes
16%
Alkyl
8%
Alternative Splicing
8%
Autosomal Recessive
11%
Blood Phenylalanine
7%
Carrier Detection
7%
Congenital Ichthyosis
9%
Cultured Fibroblasts
9%
Diet Therapy
9%
ELOVL4
7%
Erythrocytes
7%
Ether Lipid Metabolism
7%
Fatty Acids
15%
Fatty Alcohols
38%
Fatty Aldehyde Dehydrogenase
51%
Fetal Skin
9%
Fibroblasts
8%
Functional Magnetic Resonance Imaging
7%
Genome-wide Expression
7%
Glycerolipids
10%
Ichthyosis
15%
Inherited Defect
7%
Intellectual Disability
15%
Intrathecal Baclofen Therapy
7%
Lipid Peak
11%
Lipids
10%
Lorenzo's Oil
14%
Multilamellar
10%
Mutation Analysis
7%
Octadecanol
8%
Oleic Acid
14%
Oxidoreductase
9%
Pangenome Graph
7%
Pegvaliase
7%
Polyunsaturated Fatty Acids
8%
Proton MR Spectroscopy
7%
RhGAA
7%
Spastic Diplegia
16%
Spastic Tetraplegia
16%
Stratum Corneum
10%
Structure Analysis
7%
Unsaturated Aldehyde
18%
White Matter Disease
8%
Medicine and Dentistry
Adrenoleukodystrophy
22%
Alcohol Derivative
11%
Aldehyde
11%
Aldehyde Dehydrogenase
30%
Amniocyte
11%
Autosomal Recessive Disorder
7%
Biogenesis
10%
Bone Density
7%
Brain Malformation
7%
Clinical Feature
7%
Congenital Ichthyosiform Erythroderma
7%
Cross Sectional Study
7%
Cysteamine
7%
Cystinosis
7%
Cystinuria
7%
Disease
32%
Enzyme Chemistry
7%
Fatty Alcohol
22%
Genetic Disorder
16%
Hypospadias
7%
Ichthyosis
38%
Leukodystrophy
11%
Limb Defect
7%
Lorenzo Oil
14%
Maculopathy
11%
Magnetic Resonance Imaging of the Brain
7%
Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency
7%
Multiple Sulfatase Deficiency
7%
Neurologic Disease
10%
Newborn Screening
8%
Nicotinamide
7%
Nuclear Magnetic Resonance Spectroscopy
7%
Osmotic Nephrosis
7%
Oxidoreductase
16%
Peroxisomal Disorder
7%
Peroxisome
11%
Phakomatosis
13%
Polydactyly
7%
Postnatal Growth
7%
Prenatal Diagnosis
8%
Prenatal Growth
7%
Prevalence
8%
Sjögren-Larsson Syndrome
29%
Spastic Diplegia
11%
Spasticity
23%
Spectrum Disorder
14%
Symptom
17%
Visual Pigment
7%
Water-Electrolyte Imbalance
7%
Zellweger Syndrome
7%