MeSH Treeview
Query OMIM entry list
300071
CSNB2A
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
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Eye Diseases
Eye Diseases, Hereditary
Retinitis Pigmentosa
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Vision Disorders
Night Blindness
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Retinitis Pigmentosa
Genetic Diseases, X-Linked
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