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219000
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FRASER SYNDROME
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Chemical Phenomena
Biochemical Phenomena
Biochemical Processes
Protein Binding
Molecular Structure
Base Sequence
Molecular Conformation
Protein Conformation
Protein Structure, Tertiary
Chemical Processes
Biochemical Processes
Protein Binding
Metabolic Phenomena
Metabolism
Protein Binding
Genetic Phenomena
Consanguinity
Genetic Processes
Breeding
Inbreeding
Consanguinity
Mutagenesis
Sequence Deletion
Sequence Inversion
Chromosome Inversion
Genetic Structures
Base Sequence
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 4-5
Chromosomes, Human, Pair 4
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 9
Genome
Genome Components
Genes
Genes, Recessive
Genetic Variation
Mutation
Chromosome Aberrations
Chromosome Inversion
Frameshift Mutation
Sequence Deletion
Sequence Inversion
Chromosome Inversion
Genotype
Homozygote
Inheritance Patterns
Genes, Recessive
Phenotype
Physiological Phenomena
Physiological Processes
Growth and Development
Morphogenesis
Embryonic and Fetal Development
Fetal Development
Gestational Age
Reproductive and Urinary Physiological Phenomena
Reproductive Physiological Phenomena
Gestational Age
Reproductive Physiological Processes
Reproduction
Pregnancy
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