MeSH Treeview
Query OMIM entry list
302200
CCT
CATARACT, CONGENITAL TOTAL, WITH POSTERIOR SUTURAL OPACITIES IN HETEROZYGOTES
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Genetic Phenomena
Genetic Processes
Mutagenesis
Sequence Deletion
Chromosome Deletion
Genetic Structures
Chromosomes
Sex Chromosomes
X Chromosome
Genome
Genome Components
Genes
Genes, Recessive
Genetic Variation
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Sex Chromosome Aberrations
Sequence Deletion
Chromosome Deletion
Genotype
Inheritance Patterns
Genes, Recessive
Genetic Linkage
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
Ocular Physiological Phenomena
Visual Acuity
Database Center for Life Science
