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Disease Atlas
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Disease Atlas
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Disease Atlas
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Show Cases Added By Recency:
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All Diseases
1
I: Photoreceptor Diseases
1
IA: Isolated
1
IA1: Acquired/Progressive
IA2: Congenital/Stationary
1
IA2a: LCA
IA2b: SECORD
IA2c: ECORD
IA2d: Achromatopsia (Congenital Stationary Cone Dysfunction)
IA2e: Blue Cone Monochromacy
IA2f: Congenital Stationary Night Blindness
1
IA2fi: X-linked CSNB
IA2fii: Autosomal Dominant
IA2fiii: Autosomal Recessive with Normal Fundus
IA2fiv: Enhanced S-cone Syndrome
IA2fv: Fundus Albipunctatus
1
SR2923
| Fundus Albipunctatus | Gene: RDH5
SR731
| Fundus Albipunctatus | Gene: RLBP1
Other Congenital Stationary Night Blindness
IA2g: Congenital Stationary Synaptic Dysfunction
IB: Syndromic
II: Macular Diseases
III: Third Branch Disorders