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Query OMIM entry list
251880
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MITOCHONDRIAL DNA DEPLETION SYNDROME, HEPATOCEREBRAL FORM
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Chemical Phenomena
Biochemical Phenomena
Biochemical Processes
DNA Replication
Electron Transport
Molecular Structure
Amino Acid Sequence
Base Sequence
Molecular Conformation
Protein Conformation
Protein Structure, Tertiary
Chemical Processes
Biochemical Processes
DNA Replication
Electron Transport
Metabolic Phenomena
Metabolism
Energy Metabolism
Oxidation-Reduction
Electron Transport
Metabolic Networks and Pathways
Electron Transport
Cell Physiological Phenomena
Cell Physiological Processes
Cell Fusion
Genetic Phenomena
Consanguinity
Genetic Processes
Breeding
Inbreeding
Consanguinity
DNA Replication
Gene Expression
Gene Expression Regulation
Gene Amplification
Gene Expression Regulation, Enzymologic
Mutagenesis
Gene Amplification
Sequence Deletion
Gene Deletion
Genetic Structures
Base Sequence
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 1-3
Chromosomes, Human, Pair 2
Genetic Code
Codon
Codon, Terminator
Codon, Nonsense
Genome
Genome Components
Genes
Gene Components
Exons
Genetic Variation
Mutation
Chromosome Aberrations
Codon, Nonsense
Gene Amplification
Mutation, Missense
Point Mutation
Sequence Deletion
Gene Deletion
Polymorphism, Genetic
Genotype
Gene Dosage
Heterozygote
Homozygote
Phenotype
Database Center for Life Science
