MeSH Treeview
Query OMIM entry list
235730
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MOWAT-WILSON SYNDROME
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Chemical Phenomena
Biochemical Phenomena
Biochemical Processes
Signal Transduction
Molecular Structure
Amino Acid Sequence
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Molecular Conformation
Protein Conformation
Protein Structure, Secondary
Amino Acid Motifs
Zinc Fingers
Sequence Homology
Sequence Homology, Amino Acid
Chemical Processes
Biochemical Processes
Signal Transduction
Cell Physiological Phenomena
Cell Physiological Processes
Signal Transduction
Genetic Phenomena
Consanguinity
Gene Frequency
Genetic Processes
Breeding
Inbreeding
Consanguinity
DNA Damage
DNA Breaks
Chromosome Breakage
Mutagenesis
Amino Acid Substitution
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, 13-15
Chromosomes, Human, Pair 13
Genetic Code
Codon
Codon, Terminator
Codon, Nonsense
Genome
Genome Components
Genes
Alleles
Genes, Developmental
Genes, Homeobox
Tandem Repeat Sequences
Microsatellite Repeats
Genetic Variation
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Chromosome Breakage
Translocation, Genetic
Codon, Nonsense
Frameshift Mutation
Sequence Deletion
Chromosome Deletion
Gene Deletion
Polymorphism, Genetic
Polymorphism, Restriction Fragment Length
Polymorphism, Single Nucleotide
Polymorphism, Single-Stranded Conformational
Genotype
Haplotypes
Phenotype
Genetic Markers
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
Sequence Homology
Sequence Homology, Amino Acid
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