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Query OMIM entry list
143000
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HORNER SYNDROME, CONGENITAL
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Base Sequence
Sequence Homology
Sequence Homology, Nucleic Acid
Cell Physiological Phenomena
Cell Physiological Processes
Cell Cycle
Cell Division
Cell Nucleus Division
Meiosis
Genetic Phenomena
Genetic Processes
Biological Evolution
Evolution, Molecular
Cell Division
Cell Nucleus Division
Meiosis
Mutagenesis
Gene Duplication
Sequence Deletion
Chromosome Deletion
Genetic Structures
Base Sequence
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 16-18
Chromosomes, Human, Pair 17
Genome
Genome Components
Genes
Genes, Dominant
Genes, Neoplasm
Genes, Tumor Suppressor
Genes, Neurofibromatosis 1
Genes, Recessive
Genes, Tumor Suppressor
Genes, Neurofibromatosis 1
Genetic Variation
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Gene Duplication
Sequence Deletion
Chromosome Deletion
Inheritance Patterns
Genes, Dominant
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
Sequence Homology
Sequence Homology, Nucleic Acid
Musculoskeletal and Neural Physiological Phenomena
Nervous System Physiological Phenomena
Dominance, Cerebral
Functional Laterality
Biological Phenomena
Biological Processes
Biological Evolution
Evolution, Molecular
Database Center for Life Science
