MeSH Treeview
Query OMIM entry list
300352
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CREATINE DEFICIENCY SYNDROME, X-LINKED
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Chemical Phenomena
Biochemical Phenomena
Biochemical Processes
RNA Processing, Post-Transcriptional
RNA Splicing
Alternative Splicing
Molecular Structure
Amino Acid Sequence
Base Sequence
Sequence Homology
Sequence Homology, Amino Acid
Chemical Processes
Biochemical Processes
RNA Processing, Post-Transcriptional
RNA Splicing
Alternative Splicing
Metabolic Phenomena
Metabolism
RNA Processing, Post-Transcriptional
RNA Splicing
Alternative Splicing
Genetic Phenomena
Genetic Processes
Gene Expression Regulation
RNA Processing, Post-Transcriptional
RNA Splicing
Alternative Splicing
Mutagenesis
Amino Acid Substitution
Sequence Deletion
Gene Deletion
Genetic Structures
Base Sequence
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, X
Sex Chromosomes
X Chromosome
Chromosomes, Human, X
Genetic Code
Codon
Codon, Terminator
Codon, Nonsense
Genome
Genome Components
DNA, Intergenic
Introns
Genes
Gene Components
Introns
Genes, Recessive
Genetic Variation
Mutation
Codon, Nonsense
Sequence Deletion
Gene Deletion
Genotype
Genetic Predisposition to Disease
Heterozygote
Inheritance Patterns
Genes, Recessive
Genetic Linkage
Sequence Homology
Sequence Homology, Amino Acid
Database Center for Life Science
