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101600
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PFEIFFER SYNDROME
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Chemical Phenomena
Biochemical Phenomena
Biochemical Processes
RNA Processing, Post-Transcriptional
RNA Splicing
Alternative Splicing
Molecular Structure
Amino Acid Sequence
Base Sequence
Molecular Conformation
Protein Conformation
Protein Structure, Tertiary
Chemical Processes
Biochemical Processes
RNA Processing, Post-Transcriptional
RNA Splicing
Alternative Splicing
Metabolic Phenomena
Metabolism
RNA Processing, Post-Transcriptional
RNA Splicing
Alternative Splicing
Genetic Phenomena
Gene Frequency
Genetic Processes
Gene Expression Regulation
RNA Processing, Post-Transcriptional
RNA Splicing
Alternative Splicing
Mutagenesis
Amino Acid Substitution
Sequence Deletion
Recombination, Genetic
Homologous Recombination
Crossing Over, Genetic
Genetic Structures
Base Sequence
Chromosome Structures
Centromere
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 8
Chromosomes, Human, Pair 10
Genetic Code
Codon
Genome
Genome Components
DNA, Intergenic
Introns
Genes
Alleles
Gene Components
Codon
Exons
Introns
Genes, Dominant
Genetic Variation
Genetic Heterogeneity
Mutation
Chromosome Aberrations
Germ-Line Mutation
Point Mutation
Sequence Deletion
Polymorphism, Genetic
Polymorphism, Restriction Fragment Length
Polymorphism, Single-Stranded Conformational
Genotype
Genetic Predisposition to Disease
Inheritance Patterns
Genes, Dominant
Genetic Linkage
Lod Score
Phenotype
Physiological Phenomena
Physiological Processes
Growth and Development
Aging
Database Center for Life Science
