Table.

Retinal Diseases and Phenotypes Observed in this Study

Pathology, n	A	B	C	D	E	F	G
Achromatopsia, 5	X	X	X
Acquired optic disc pit, 1	X		X	X
Acute macular neuroretinopathy, 1							X
AMD, 2			X	X
Astrocytic hamartoma, 1			X		X		X
Autoimmune retinopathy, 1			X
Best disease, 2	X					X	X
Birdshot choroidoretinopathy, 4	X		X	X
Bornholm eye disease, 1	X
BRAO & BRVO, 3	X	X	X
Central retinal artery occlusion, 1	X			X
Central serous retinopathy, 3	X	X	X	X	X		X
Choroideremia, 8	X			X	X		X
Color blindness, 1	X	X
Commotio retinae, 5	X	X				X	X
Cone dystrophy, 4	X		X	X			X
Cotton-wool spot, 1		X
Diabetic retinopathy, 2	X	X			X
Epiretinal membrane, 2		X	X
Free of disease, 11	X	X		X
Glaucoma, 11	X	X	X	X
Leber's congenital amaurosis, 2	X			X	X
Leber's hereditary optic neuropathy, 1	X	X
Macular hole, 4	X	X	X	X	X	X
Macular telangiectasia, 7	X		X		X	X
Microscotoma, 3	X	X	X
Multiple sclerosis, 1	X	X
Optic atrophy, 5	X	X	X	X	X	X
Optic nerve drusen, 2		X
Optic neuritis, 3						X
Parkinson's disease, 3	X	X	X	X	X		X
Pathologic myopia, 1				X
Premature birth, 1	X
Retinitis pigmentosa, 4	X	X	X	X	X
Retinoschisis, 1		X				X	X
Rubella retinopathy, 1	X		X		X
Stargardt, 1					X
Traumatic brain injury, 1						X
Unknown retinopathy, 1		X					X

The columns represent each of the seven findings described here; an “X” indicates that it was observed in our cohort. The absence of a feature (no “X”) should not be interpreted as an absolute absence, rather not yet observed. A, punctate reflectivity; B, nummular (disc-shaped) reflectivity; C, granular membrane; D, waxy membrane; E, vessel associated membrane; F, microcysts; G, striate reflectivity.