MeSH Treeview
Query OMIM entry list
180071
PDE6A
PHOSPHODIESTERASE 6A, cGMP-SPECIFIC, ROD, ALPHA
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Eye Diseases
Eye Diseases, Hereditary
Retinitis Pigmentosa
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Retinitis Pigmentosa
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