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Query OMIM entry list
600649
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CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Base Sequence
Molecular Conformation
Protein Conformation
Protein Structure, Secondary
Metabolic Phenomena
Metabolism
Energy Metabolism
Genetic Phenomena
Genetic Processes
Mutagenesis
Sequence Deletion
Chromosome Deletion
Genetic Structures
Base Sequence
Genome
Genome Components
Genes
Alleles
Genetic Variation
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Point Mutation
Sequence Deletion
Chromosome Deletion
Polymorphism, Genetic
Genotype
Heterozygote
Homozygote
Phenotype
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
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