MeSH Treeview
Query OMIM entry list
300672
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RETT SYNDROME, ATYPICAL, CDKL5-RELATED
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Genetic Phenomena
Genetic Processes
Gene Expression Regulation
Epigenesis, Genetic
Dosage Compensation, Genetic
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, X
Sex Chromosomes
X Chromosome
Chromosomes, Human, X
Genome
Genome Components
Tandem Repeat Sequences
Microsatellite Repeats
Genetic Variation
Mutation
Mutation, Missense
Genotype
Genetic Predisposition to Disease
Haplotypes
Database Center for Life Science
