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Gyrate atrophy of the choroid and retina, shortened to gyrate atrophy, is an inherited disorder of protein metabolism characterised by progressive vision loss.

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Usher syndrome is an inherited condition that affects both hearing and vision.

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Stargardt disease is the most common form of juvenile macular dystrophy (or inherited degeneration).

Bardet-Biedl syndrome (BBS) is an inherited condition which impacts many parts of the body including the retina.

Achromatopsia is a rare hereditary vision disorder affecting approximately 1 in 30,000 newborn babies.

Leber Congenital Amaurosis (LCA) is a rare genetic eye disease that appears at birth or in the first few months of life.

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