Medicine and Dentistry
Phenotype
100%
Oxidoreductase
33%
Gene
33%
Diseases
16%
Congenital Malformation
16%
Brain Disease
16%
Cerebrospinal Fluid
16%
Epigenomics
16%
Urine
16%
Epilepsy
16%
Water-Electrolyte Imbalance
16%
Autosomal Recessive Inheritance
16%
Developmental Delay
16%
Monozygotic Twins
16%
Phenotypic Variation
16%
Female
16%
Mutant
16%
Blood
16%
Base
16%
Environmental Factor
16%
Sibling
16%
Biochemistry, Genetics and Molecular Biology
Phenotype
100%
Oxidoreductase
66%
Nested Gene
33%
Mutation
33%
Metabolic Disorder
33%
Allele
16%
Gene Mutation
16%
Autosomal Recessive Inheritance
16%
Phenotypic Variation
16%
Mutant
16%
Phenotypic Heterogeneity
16%
Monozygotic Twins
16%
Immunology and Microbiology
Phenotype
100%
Mutation
33%
Gene
33%
Allele
16%
Epigenetics
16%
Blood Product
16%
Cerebrospinal Fluid
16%
Urine
16%
Autosomal Recessive Inheritance
16%
Monozygotic Twins
16%
Mutant
16%
Heterozygote
16%
Neuroscience
Phenotype
100%
Gene
33%
Epigenetics
16%
Encephalopathy
16%
Pharmacology, Toxicology and Pharmaceutical Science
Aciduria
83%
2 Hydroxyglutaric Acid
50%