MeSH Treeview
Query OMIM entry list
605711
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MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME
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High-scoring List
Genetic Phenomena
Genetic Processes
Mutagenesis
Sequence Deletion
Chromosome Deletion
Genetic Structures
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 1-3
Chromosomes, Human, Pair 2
Genome
Genome Components
Sequence Tagged Sites
Genetic Variation
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Sequence Deletion
Chromosome Deletion
Phenotype
Genetic Markers
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
Diploidy
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