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Query OMIM entry list
248950
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MCDONOUGH SYNDROME
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Genetic Phenomena
Genetic Processes
Mutagenesis
Translocation, Genetic
Genetic Structures
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 19-20
Sex Chromosomes
X Chromosome
Genetic Variation
Mutation
Chromosome Aberrations
Aneuploidy
Translocation, Genetic
Genotype
Heterozygote
Ploidies
Aneuploidy
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