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Query OMIM entry list
604757
CRS2
CRANIOSYNOSTOSIS, TYPE 2
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
DNA, Satellite
Conserved Sequence
Sequence Homology
Sequence Homology, Amino Acid
Genetic Phenomena
Gene Frequency
Genetic Processes
Mutagenesis
Sequence Deletion
Chromosome Deletion
Recombination, Genetic
Genetic Structures
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
DNA, Satellite
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 4-5
Chromosomes, Human, Pair 5
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 12
Chromosomes, Human, 16-18
Chromosomes, Human, Pair 16
Genome
Genome Components
DNA, Intergenic
DNA, Satellite
Genes
Alleles
Genes, Developmental
Genes, Homeobox
Genes, Dominant
Tandem Repeat Sequences
DNA, Satellite
Genetic Variation
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Trisomy
Chromosome Duplication
Trisomy
Sequence Deletion
Chromosome Deletion
Polymorphism, Genetic
Inheritance Patterns
Genes, Dominant
Genetic Linkage
Phenotype
Genetic Markers
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
Trisomy
Sequence Homology
Sequence Homology, Amino Acid
Database Center for Life Science