MeSH Treeview
Query OMIM entry list
300071
CSNB2A
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Sequence Homology
Sequence Homology, Amino Acid
Metabolic Phenomena
Pharmacokinetics
Tissue Distribution
Genetic Phenomena
Gene Order
Genetic Processes
Gene Expression
Recombination, Genetic
Transfection
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
Genome
Genome Components
Genes
Gene Components
Exons
Genetic Variation
Mutation
Polymorphism, Genetic
Polymorphism, Single-Stranded Conformational
Genotype
Haplotypes
Genetic Linkage
Lod Score
Phenotype
Genetic Markers
Sequence Homology
Sequence Homology, Amino Acid
Physiological Phenomena
Pharmacological Phenomena
Pharmacokinetics
Tissue Distribution
Ocular Physiological Phenomena
Visual Acuity
Database Center for Life Science
