MeSH Treeview
Query OMIM entry list
611644
HSCR9
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 9
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Base Sequence
Regulatory Sequences, Nucleic Acid
Promoter Regions, Genetic
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Conserved Sequence
Consensus Sequence
Genetic Phenomena
Gene Frequency
Genetic Structures
Base Sequence
Regulatory Sequences, Nucleic Acid
Promoter Regions, Genetic
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 4-5
Chromosomes, Human, Pair 4
Genome
Genome Components
Genes
Gene Components
Exons
Regulatory Elements, Transcriptional
Promoter Regions, Genetic
Genes, Dominant
Tandem Repeat Sequences
Microsatellite Repeats
Genetic Variation
Mutation
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Genotype
Genetic Predisposition to Disease
Haplotypes
Inheritance Patterns
Genes, Dominant
Genetic Linkage
Linkage Disequilibrium
Phenotype
Genetic Markers
Mathematical Concepts
Probability
Risk
Database Center for Life Science
