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Query OMIM entry list
244460
KCS
KENNY-CAFFEY SYNDROME, TYPE 1
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Sequence Homology
Sequence Homology, Amino Acid
Metabolic Phenomena
Pharmacokinetics
Tissue Distribution
Genetic Phenomena
Consanguinity
Genetic Processes
Breeding
Inbreeding
Consanguinity
Mutagenesis
Sequence Deletion
Chromosome Deletion
Gene Deletion
Genetic Structures
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 1-3
Chromosomes, Human, Pair 1
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 9
Chromosomes, Human, 21-22 and Y
Chromosomes, Human, Pair 22
Genome
Genome Components
Genes
Genes, Recessive
Tandem Repeat Sequences
Genetic Variation
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Mutation, Missense
Sequence Deletion
Chromosome Deletion
Gene Deletion
Genotype
Haplotypes
Homozygote
Inheritance Patterns
Genes, Recessive
Genetic Linkage
Lod Score
Phenotype
Genetic Markers
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
Sequence Homology
Sequence Homology, Amino Acid
Physiological Phenomena
Pharmacological Phenomena
Pharmacokinetics
Tissue Distribution
Ocular Physiological Phenomena
Intraocular Pressure
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