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