MeSH Treeview
Query OMIM entry list
600325
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AMINOPTERIN SYNDROME SINE AMINOPTERIN
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High-scoring List
Genetic Phenomena
Consanguinity
Genetic Processes
Breeding
Inbreeding
Consanguinity
Mutagenesis
Translocation, Genetic
Genetic Structures
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 4-5
Chromosomes, Human, Pair 5
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 10
Genetic Variation
Mutation
Chromosome Aberrations
Mosaicism
Translocation, Genetic
Reproductive and Urinary Physiological Phenomena
Reproductive Physiological Phenomena
Reproductive Physiological Processes
Reproduction
Pregnancy
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