MeSH Treeview
Query OMIM entry list
602081
SPCH1
SPEECH-LANGUAGE DISORDER 1
→
High-scoring List
Chemical Phenomena
Biochemical Phenomena
Biochemical Processes
RNA Processing, Post-Transcriptional
RNA Splicing
Alternative Splicing
Molecular Structure
Amino Acid Sequence
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Molecular Conformation
Protein Conformation
Protein Structure, Tertiary
Sequence Homology
Sequence Homology, Amino Acid
Sequence Homology, Nucleic Acid
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
DNA Damage
DNA Breaks
Chromosome Breakage
Gene Expression
Gene Expression Regulation
Epigenesis, Genetic
Genomic Imprinting
RNA Processing, Post-Transcriptional
RNA Splicing
Alternative Splicing
Mutagenesis
Sequence Deletion
Chromosome Deletion
Gene Deletion
Translocation, Genetic
Genetic Structures
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 1-3
Chromosomes, Human, Pair 2
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 7
Chromosomes, Human, 13-15
Chromosomes, Human, Pair 13
Chromosomes, Human, 16-18
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 17
Chromosomes, Human, 19-20
Chromosomes, Human, Pair 19
Sex Chromosomes
X Chromosome
Genetic Code
Codon
Codon, Initiator
Codon, Terminator
Codon, Nonsense
Genome
Genome Components
DNA, Intergenic
Introns
Genes
Alleles
Gene Components
Codon
Codon, Initiator
Codon, Terminator
Exons
Expressed Sequence Tags
Introns
Genes, Dominant
Genes, Recessive
Sequence Tagged Sites
Tandem Repeat Sequences
Microsatellite Repeats
Genome, Human
Genetic Variation
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Chromosome Breakage
Translocation, Genetic
Uniparental Disomy
Codon, Nonsense
Point Mutation
Sequence Deletion
Chromosome Deletion
Gene Deletion
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Genotype
Genetic Predisposition to Disease
Haplotypes
Heterozygote
Inheritance Patterns
Genes, Dominant
Genes, Recessive
Quantitative Trait, Heritable
Genetic Linkage
Lod Score
Phenotype
Genetic Markers
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
Sequence Homology
Sequence Homology, Amino Acid
Sequence Homology, Nucleic Acid
Musculoskeletal and Neural Physiological Phenomena
Nervous System Physiological Phenomena
Dominance, Cerebral
Functional Laterality
Nervous System Physiological Processes
Speech
Speech Intelligibility
Database Center for Life Science
