Any retinitis pigmentosa in which the cause of the disease is a mutation in the FSCN2 gene.
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
retinitis pigmentosa 6
MONDO:0000910
cone-rod dystrophy 2
MONDO:0007362
retinitis pigmentosa 1
MONDO:0008377
retinitis pigmentosa 9
MONDO:0008378
retinitis pigmentosa 10
MONDO:0008379
dominant pericentral pigmentary retinopathy
MONDO:0008381