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Query OMIM entry list
609460
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GOLDBERG-SHPRINTZEN MEGACOLON SYNDROME
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Base Sequence
Genetic Phenomena
Consanguinity
Genetic Processes
Breeding
Inbreeding
Consanguinity
Mutagenesis
Amino Acid Substitution
Genetic Structures
Base Sequence
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 10
Genetic Code
Codon
Codon, Terminator
Codon, Nonsense
Genome
Genome Components
Genes
Genes, Recessive
Genetic Variation
Mutation
Codon, Nonsense
Frameshift Mutation
Inheritance Patterns
Genes, Recessive
Phenotype
Database Center for Life Science