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Query OMIM entry list
148820
WS3
WAARDENBURG SYNDROME, TYPE III
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Molecular Conformation
Protein Conformation
Protein Structure, Secondary
Sequence Homology
Sequence Homology, Amino Acid
Genetic Phenomena
Consanguinity
Genetic Processes
Breeding
Inbreeding
Consanguinity
Gene Expression Regulation
Mutagenesis
Sequence Deletion
Chromosome Deletion
Genetic Structures
Base Sequence
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 1-3
Chromosomes, Human, Pair 2
Gene Library
Genetic Vectors
Cosmids
Genome
Genome Components
Genes
Gene Components
Exons
Genes, Developmental
Genes, Homeobox
Genes, Dominant
Genes, Recessive
Plasmids
Cosmids
Genetic Variation
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Sequence Deletion
Chromosome Deletion
Genotype
Homozygote
Inheritance Patterns
Genes, Dominant
Genes, Recessive
Genetic Linkage
Phenotype
Genetic Markers
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
Sequence Homology
Sequence Homology, Amino Acid
Physiological Phenomena
Physiological Processes
Homeostasis
Reproductive and Urinary Physiological Phenomena
Reproductive Physiological Phenomena
Reproductive Physiological Processes
Reproduction
Pregnancy
Musculoskeletal and Neural Physiological Phenomena
Nervous System Physiological Phenomena
Nervous System Physiological Processes
Sensation
Hearing
Integumentary System Physiological Phenomena
Hair Color
Biological Phenomena
Pigmentation
Hair Color
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