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123500
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CROUZON SYNDROME
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Chemical Phenomena
Biochemical Phenomena
Biochemical Processes
Signal Transduction
Molecular Structure
Amino Acid Sequence
Base Sequence
Conserved Sequence
Consensus Sequence
Sequence Homology
Sequence Homology, Amino Acid
Chemical Processes
Biochemical Processes
Signal Transduction
Cell Physiological Phenomena
Cell Physiological Processes
Signal Transduction
Genetic Phenomena
Gene Frequency
Genetic Processes
Gene Expression Regulation
Genetic Structures
Base Sequence
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 10
Genome
Genome Components
DNA, Intergenic
Introns
Genes
Alleles
Gene Components
Exons
Introns
Genes, Dominant
Genes, Recessive
Genetic Variation
Genetic Heterogeneity
Mutation
Chromosome Aberrations
Mosaicism
Germ-Line Mutation
Point Mutation
Polymorphism, Genetic
Polymorphism, Single-Stranded Conformational
Genotype
Genetic Predisposition to Disease
Inheritance Patterns
Genes, Dominant
Genes, Recessive
Genetic Linkage
Lod Score
Phenotype
Genetic Markers
Sequence Homology
Sequence Homology, Amino Acid
Physiological Phenomena
Physiological Processes
Growth and Development
Aging
Reproductive and Urinary Physiological Phenomena
Reproductive Physiological Phenomena
Maternal Age
Reproductive Physiological Processes
Reproduction
Pregnancy
Biological Phenomena
Species Specificity
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