MeSH Treeview
Query OMIM entry list
608983
CCA3
CATARACT, CONGENITAL, CERULEAN TYPE, 3
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High-scoring List
Eye Diseases
Lens Diseases
Cataract
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Genetic Diseases, Inborn
Chromosome Disorders
Database Center for Life Science
