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Query OMIM entry list
601399
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PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Sequence Homology
Sequence Homology, Amino Acid
Sequence Homology, Nucleic Acid
Cell Physiological Phenomena
Cell Physiological Processes
Cell Differentiation
Hematopoiesis
Genetic Phenomena
Genetic Processes
Mutagenesis
Sequence Deletion
Genetic Structures
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 7
Chromosomes, Human, Pair 8
Chromosomes, Human, 21-22 and Y
Chromosomes, Human, Pair 21
Genome
Genome Components
Genes
Genes, Dominant
Genes, Neoplasm
Oncogenes
Tandem Repeat Sequences
Microsatellite Repeats
Genetic Variation
Genetic Heterogeneity
Mutation
Chromosome Aberrations
Aneuploidy
Monosomy
Trisomy
Chromosome Duplication
Trisomy
Sequence Deletion
Genotype
Genetic Predisposition to Disease
Haplotypes
Heterozygote
Inheritance Patterns
Genes, Dominant
Genetic Linkage
Lod Score
Phenotype
Genetic Markers
Ploidies
Aneuploidy
Monosomy
Trisomy
Sequence Homology
Sequence Homology, Amino Acid
Sequence Homology, Nucleic Acid
Physiological Phenomena
Body Constitution
Disease Susceptibility
Circulatory and Respiratory Physiological Phenomena
Blood Physiological Phenomena
Blood Physiological Processes
Hematopoiesis
Mathematical Concepts
Probability
Risk
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