Disease_Mapped_To_Gene Macular Degeneration Cellosaurus Disease Terminology ABCA4 Gene ELOVL4 Gene Rare Non-Neoplastic Disorder PROM1 Gene Stargardt Disease Disease or Syndrome An autosomal recessive and rarely autosomal dominant inherited disorder caused by mutations in the ABCA4 or ELOVL4 genes respectively. It is characterized by macular degeneration that begins in late childhood resulting in progressive loss of vision. Cellosaurus C85078 Stargardt Disease C0271093 Stargardt Disease