MeSH Treeview
Query OMIM entry list
608983
CCA3
CATARACT, CONGENITAL, CERULEAN TYPE, 3
→
High-scoring List
Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Sequence Homology
Sequence Homology, Amino Acid
Genetic Phenomena
Genetic Structures
Base Sequence
Repetitive Sequences, Nucleic Acid
Tandem Repeat Sequences
Microsatellite Repeats
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 1-3
Chromosomes, Human, Pair 2
Chromosomes, Human, 16-18
Chromosomes, Human, Pair 17
Chromosomes, Human, 21-22 and Y
Chromosomes, Human, Pair 22
Genome
Genome Components
Genes
Genes, Dominant
Tandem Repeat Sequences
Microsatellite Repeats
Genetic Variation
Genetic Heterogeneity
Mutation
Mutation, Missense
Genotype
Haplotypes
Inheritance Patterns
Genes, Dominant
Genetic Linkage
Lod Score
Phenotype
Genetic Markers
Sequence Homology
Sequence Homology, Amino Acid
Database Center for Life Science
