Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Eye Diseases, Hereditary » Retinitis Pigmentosa
Hereditary, progressive degeneration of the retina due to death of ROD PHOTORECEPTORS initially and subsequent death of CONE PHOTORECEPTORS. It is characterized by deposition of pigment in the retina. MeSH
Phase 2 Indicated Drugs (21)
Organization Involved with Phase 2 Indications (52)
Organization Involved with Phase 1 Indications (17)
Organization Involved with Other Experimental Indications (1)
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