Any Stargardt disease in which the cause of the disease is a mutation in the PROM1 gene.
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
severe early-childhood-onset retinal dystrophy
MONDO:0009549
Stargardt disease 3
MONDO:0010819
retinal macular dystrophy type 2
MONDO:0011957