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Query OMIM entry list
236270
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HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA DUE TO DEFECT IN COBALAMIN METABOLISM, cblE COMPLEMENTATION TYPE
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Base Sequence
Genetic Phenomena
Genetic Processes
Mutagenesis
Amino Acid Substitution
Sequence Deletion
Recombination, Genetic
Transfection
Genetic Structures
Base Sequence
Genetic Code
Codon
Codon, Terminator
Codon, Nonsense
Genome
Genome Components
Genes
Genes, Synthetic
Genetic Variation
Mutation
Codon, Nonsense
Mutation, Missense
Point Mutation
Sequence Deletion
Polymorphism, Genetic
Polymorphism, Restriction Fragment Length
Genotype
Haplotypes
Circulatory and Respiratory Physiological Phenomena
Blood Physiological Phenomena
Erythrocyte Indices
Database Center for Life Science
