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Query OMIM entry list
601499
RIEG2
RIEGER SYNDROME, TYPE 2
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Repetitive Sequences, Nucleic Acid
Interspersed Repetitive Sequences
DNA Transposable Elements
Genetic Phenomena
Genetic Processes
Gene Expression
Mutagenesis
Gene Duplication
Sequence Deletion
Chromosome Deletion
Genetic Structures
Base Sequence
Repetitive Sequences, Nucleic Acid
Interspersed Repetitive Sequences
DNA Transposable Elements
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 6
Chromosomes, Human, 13-15
Chromosomes, Human, Pair 13
Genetic Code
Codon
Codon, Terminator
Codon, Nonsense
Genome
Genome Components
Genes
Genes, Dominant
Interspersed Repetitive Sequences
DNA Transposable Elements
Genetic Variation
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Codon, Nonsense
Gene Duplication
Sequence Deletion
Chromosome Deletion
Genotype
Gene Dosage
Inheritance Patterns
Genes, Dominant
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
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