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176450
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CURRARINO SYNDROME
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Conserved Sequence
Genetic Phenomena
Genetic Processes
Mutagenesis
Amino Acid Substitution
Sequence Deletion
Chromosome Deletion
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 1
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 7
Genetic Code
Codon
Codon, Terminator
Genome
Genome Components
Genes
Gene Components
Codon
Codon, Terminator
Genes, Developmental
Genes, Homeobox
Genes, Dominant
Tandem Repeat Sequences
Microsatellite Repeats
Genetic Variation
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Frameshift Mutation
Mutation, Missense
Sequence Deletion
Chromosome Deletion
Genotype
Haplotypes
Inheritance Patterns
Genes, Dominant
Genetic Linkage
Lod Score
Phenotype
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
Physiological Phenomena
Physiological Processes
Growth and Development
Morphogenesis
Database Center for Life Science
