MeSH Treeview
Query OMIM entry list
600666
PKD3
POLYCYSTIC KIDNEY DISEASE 3, AUTOSOMAL DOMINANT
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Regulatory Sequences, Nucleic Acid
Regulatory Sequences, Ribonucleic Acid
RNA Splice Sites
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Genetic Phenomena
Genetic Processes
Mutagenesis
Sequence Deletion
Gene Deletion
Recombination, Genetic
Genetic Structures
Base Sequence
Regulatory Sequences, Nucleic Acid
Regulatory Sequences, Ribonucleic Acid
RNA Splice Sites
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 1-3
Chromosomes, Human, Pair 2
Chromosomes, Human, 4-5
Chromosomes, Human, Pair 4
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 8
Chromosomes, Human, 16-18
Chromosomes, Human, Pair 16
Genetic Code
Codon
Codon, Terminator
Codon, Nonsense
Reading Frames
Open Reading Frames
Genome
Genome Components
Genes
Gene Components
Open Reading Frames
RNA Splice Sites
Genes, Dominant
Tandem Repeat Sequences
Microsatellite Repeats
Genetic Variation
Genetic Heterogeneity
Mutation
Codon, Nonsense
Frameshift Mutation
Mutation, Missense
Sequence Deletion
Gene Deletion
Polymorphism, Genetic
Polymorphism, Restriction Fragment Length
Genotype
Haplotypes
Heterozygote
Inheritance Patterns
Genes, Dominant
Genetic Linkage
Lod Score
Phenotype
Genetic Markers
Physiological Phenomena
Body Constitution
Body Weights and Measures
Body Size
Body Weight
Organ Size
Physiological Processes
Growth and Development
Growth
Body Size
Body Weight
Organ Size
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