MeSH Treeview
Query OMIM entry list
608462
HSCR8
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 8
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Genetic Phenomena
Genetic Processes
Gene Expression Regulation
Epistasis, Genetic
Genetic Structures
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 10
Chromosomes, Human, 13-15
Chromosomes, Human, Pair 13
Chromosomes, Human, 16-18
Chromosomes, Human, Pair 16
Genome
Genome Components
Tandem Repeat Sequences
Microsatellite Repeats
Genetic Variation
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Genetic Linkage
Linkage Disequilibrium
Lod Score
Phenotype
Genetic Markers
Database Center for Life Science
