MeSH Treeview
Query OMIM entry list
604485
NR2E3
NUCLEAR RECEPTOR SUBFAMILY 2, GROUP E, MEMBER 3
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Eye Diseases
Eye Abnormalities
Retinal Dysplasia
Eye Diseases, Hereditary
Retinal Dysplasia
Retinitis Pigmentosa
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Retinal Dysplasia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Eye Abnormalities
Retinal Dysplasia
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Retinal Dysplasia
Retinitis Pigmentosa
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease
Syndrome
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