MeSH Treeview
Query OMIM entry list
302200
CCT
CATARACT, CONGENITAL TOTAL, WITH POSTERIOR SUTURAL OPACITIES IN HETEROZYGOTES
→
High-scoring List
Nervous System Diseases
Cranial Nerve Diseases
Ocular Motility Disorders
Nystagmus, Pathologic
Eye Diseases
Eye Abnormalities
Microphthalmos
Lens Diseases
Cataract
Ocular Motility Disorders
Nystagmus, Pathologic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Eye Abnormalities
Microphthalmos
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Sex Chromosome Aberrations
Database Center for Life Science
