MeSH Treeview
Query OMIM entry list
608638
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ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1
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High-scoring List
Genetic Phenomena
Genetic Structures
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 1-3
Chromosomes, Human, Pair 3
Chromosomes, Human, 16-18
Chromosomes, Human, Pair 17
Genetic Variation
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Genotype
Genetic Predisposition to Disease
Haplotypes
Phenotype
Database Center for Life Science
