MeSH Treeview
Query OMIM entry list
300486
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MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE
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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
Regulatory Sequences, Nucleic Acid
Regulatory Sequences, Ribonucleic Acid
RNA Splice Sites
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
DNA Damage
DNA Breaks
Chromosome Breakage
Gene Expression Regulation
Epigenesis, Genetic
Dosage Compensation, Genetic
Gene Expression Regulation, Developmental
RNA Processing, Post-Transcriptional
RNA Splicing
Alternative Splicing
Mutagenesis
Sequence Deletion
Gene Deletion
Translocation, Genetic
Genetic Structures
Base Sequence
Regulatory Sequences, Nucleic Acid
Regulatory Sequences, Ribonucleic Acid
RNA Splice Sites
Chromosomes
Chromosomes, Artificial
Chromosomes, Artificial, Yeast
Chromosomes, Fungal
Chromosomes, Artificial, Yeast
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 12
Chromosomes, Human, X
Sex Chromosomes
X Chromosome
Chromosomes, Human, X
Genetic Code
Codon
Codon, Terminator
Codon, Nonsense
Genetic Vectors
Chromosomes, Artificial
Chromosomes, Artificial, Yeast
Cosmids
Genome
Genome Components
Genes
Gene Components
RNA Splice Sites
Plasmids
Cosmids
Genetic Variation
Mutation
Chromosome Aberrations
Chromosome Breakage
Translocation, Genetic
Codon, Nonsense
Frameshift Mutation
Sequence Deletion
Gene Deletion
Genotype
Heterozygote
Genetic Linkage
Phenotype
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