MeSH Treeview
Query OMIM entry list
610427
CSNB2B
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Genetic Phenomena
Genetic Processes
Mutagenesis
Sequence Deletion
Gene Deletion
Genetic Structures
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 11
Genome
Genome Components
Genes
Gene Components
Exons
Genes, Recessive
Genetic Variation
Mutation
Mutation, Missense
Sequence Deletion
Gene Deletion
Inheritance Patterns
Genes, Recessive
Ocular Physiological Phenomena
Visual Acuity
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