MeSH Treeview
Query OMIM entry list
115660
CCA1
CATARACT, CONGENITAL, CERULEAN TYPE, 1
→
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
Consanguinity
Genetic Processes
Breeding
Inbreeding
Consanguinity
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, 19-20
Chromosomes, Human, Pair 19
Genetic Code
Codon
Codon, Terminator
Codon, Nonsense
Genome
Genome Components
Genes
Gene Components
Exons
Genes, Dominant
Genes, Recessive
Tandem Repeat Sequences
Microsatellite Repeats
Genetic Variation
Mutation
Codon, Nonsense
Mutation, Missense
Genotype
Haplotypes
Homozygote
Inheritance Patterns
Genes, Dominant
Genes, Recessive
Genetic Linkage
Lod Score
Phenotype
Genetic Markers
Sequence Homology
Sequence Homology, Amino Acid
Physiological Phenomena
Physiological Processes
Growth and Development
Aging
Database Center for Life Science
