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Query OMIM entry list
603285
CCM3
CEREBRAL CAVERNOUS MALFORMATIONS 3
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
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
Chromosome Deletion
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 3
Chromosomes, Human, 4-5
Chromosomes, Human, Pair 5
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 7
Genetic Code
Codon
Codon, Terminator
Codon, Nonsense
Genome
Genome Components
Genes
Gene Components
Exons
RNA Splice Sites
Tandem Repeat Sequences
Microsatellite Repeats
Genetic Variation
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Codon, Nonsense
Point Mutation
Sequence Deletion
Chromosome Deletion
Genotype
Genetic Predisposition to Disease
Heterozygote
Genetic Linkage
Lod Score
Phenotype
Genetic Markers
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
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