Medicine & Life Sciences
Adrenoleukodystrophy
100%
Fatty Acids
86%
Peroxisomes
81%
long-chain-fatty-acid-CoA ligase
79%
Coenzyme A Ligases
57%
Peroxisomal Disorders
48%
Phytanic Acid
34%
Fatty Acid Transport Proteins
28%
Acyl Coenzyme A
26%
ADP-Ribosylation
26%
Fibroblasts
25%
Enzymes
25%
ADP Ribose Transferases
24%
Proteins
23%
Liver
20%
phytanoyl-coenzyme A
19%
Rhizomelic Chondrodysplasia Punctata
18%
Cholera Toxin
16%
sterol carrier proteins
16%
ATP Binding Cassette Transporter, Subfamily D, Member 1
14%
Genes
14%
NAD
14%
Pertussis Toxin
13%
Acyl-CoA Oxidase
13%
Plasmalogens
13%
Refsum Disease
12%
Bile Acids and Salts
12%
Coenzyme A
12%
Turkeys
12%
Mutation
12%
Membrane Proteins
11%
Brain
11%
Ligases
11%
Lipids
11%
Adenosine Triphosphate
11%
pipecolic acid
11%
Phenotype
10%
Unsaturated Fatty Acids
10%
Erythrocytes
10%
Mitochondria
9%
Adenosine Diphosphate Ribose
9%
Peroxisomal Bifunctional Enzyme
9%
Transferases
9%
Organelles
9%
Adenosine Diphosphate
9%
Membranes
9%
Sarcosine Oxidase
9%
Gonadal dysgenesis XX type deafness
9%
Yeasts
8%
Chemical Compounds
Acyl-CoA
69%
Protein
27%
Phytanic Acid
25%
Fatty Acid
19%
Pharmacological Metabolism
14%
Toxin
14%
Phytanoyl-CoA
13%
Disorder
13%
Ribosylation
11%
Long-Chain Fatty Acid
10%
Very Long-Chain Fatty Acyl-CoA
10%
Arginine
9%
ADP
7%
Complementary DNA
6%
Branched-Chain Fatty Acid
6%
Bile Acid
6%
Mutation
5%
Nucleotide
5%
Metabolic
5%