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Query OMIM entry list
607822
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ALZHEIMER DISEASE 3
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Chemical Phenomena
Biochemical Phenomena
Biochemical Processes
RNA Processing, Post-Transcriptional
RNA Splicing
Alternative Splicing
Transcription, Genetic
Molecular Structure
Amino Acid Sequence
Base Sequence
Regulatory Sequences, Nucleic Acid
Promoter Regions, Genetic
Repetitive Sequences, Nucleic Acid
Molecular Conformation
Protein Conformation
Protein Structure, Secondary
Sequence Homology
Sequence Homology, Amino Acid
Chemical Processes
Biochemical Processes
RNA Processing, Post-Transcriptional
RNA Splicing
Alternative Splicing
Transcription, Genetic
Metabolic Phenomena
Metabolism
RNA Processing, Post-Transcriptional
RNA Splicing
Alternative Splicing
Genetic Phenomena
Founder Effect
Gene Frequency
Genetic Processes
Gene Expression
Transcription, Genetic
Gene Expression Regulation
RNA Processing, Post-Transcriptional
RNA Splicing
Alternative Splicing
Mutagenesis
Amino Acid Substitution
Mutagenesis, Insertional
Sequence Deletion
Chromosome Deletion
Recombination, Genetic
Genetic Structures
Base Sequence
Regulatory Sequences, Nucleic Acid
Promoter Regions, Genetic
Repetitive Sequences, Nucleic Acid
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 13-15
Chromosomes, Human, Pair 14
Chromosomes, Human, 21-22 and Y
Chromosomes, Human, Pair 21
Sex Chromosomes
X Chromosome
Gene Library
Genomic Library
Genetic Code
Codon
Reading Frames
Open Reading Frames
Genome
Genome Components
DNA, Intergenic
Introns
Genes
Alleles
Gene Components
Codon
Exons
Introns
Open Reading Frames
Regulatory Elements, Transcriptional
Promoter Regions, Genetic
Genes, Dominant
Genomic Library
Genetic Variation
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Chromosomal Instability
Chromosome Fragility
Mutagenesis, Insertional
Mutation, Missense
Point Mutation
Sequence Deletion
Chromosome Deletion
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Genomic Instability
Chromosomal Instability
Chromosome Fragility
Genotype
Genetic Predisposition to Disease
Haplotypes
Heterozygote
Inheritance Patterns
Genes, Dominant
Genetic Linkage
Lod Score
Phenotype
Genetic Markers
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
Sequence Homology
Sequence Homology, Amino Acid
Reproductive and Urinary Physiological Phenomena
Reproductive Physiological Phenomena
Sex Characteristics
Biological Phenomena
Ecological and Environmental Phenomena
Environment
Mathematical Concepts
Statistical Distributions
Chi-Square Distribution
Database Center for Life Science
