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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
4
I: Photoreceptor Diseases
4
IA: Isolated
4
IA1: Acquired/Progressive
IA2: Congenital/Stationary
4
IA2a: LCA
3
SR644
| Leber Congenital Amaurosis | Gene: CEP290
SR2325
| Leber Congenital Amaurosis | Gene: CEP290
SR2624
| Leber Congenital Amaurosis | Gene: CEP290
SR715
| Leber Congenital Amaurosis | Gene: CEP290
SR703
| Leber Congenital Amaurosis | Gene: AIPL1
SR82
| Leber Congenital Amaurosis | Gene: CRX
SR206
| Leber Congenital Amaurosis | Gene: NMNAT1
SR2292
| Leber Congenital Amaurosis | Gene: NMNAT1
SR561
| Leber Congenital Amaurosis | Gene: NMNAT1
SR2709
| Leber Congenital Amaurosis | Gene: GUCY2D
SR806
| Leber Congenital Amaurosis | Gene: RNU6-9
IA2b: SECORD
1
SR302
| SECORD | Gene: CEP290
SR43
| SECORD | Gene: RDH12
SR201
| SECORD | Gene: CEP290
SR2368
| SECORD | Gene: CEP290
SR1796
| SECORD | Gene: CRB1
SR263
| SECORD | Gene: CRB1
SR54
| SECORD | Gene: NMNAT1
SR2921
| SECORD | Gene: RPE65
SR741
| SECORD | Gene: RPE65
SR88
| SECORD | Gene: RPE65
SR627
| SECORD | Gene: RPGRIP1
SR306
| SECORD | Gene: LCA5
SR2702
| SECORD | Gene: OTX2
IA2c: ECORD
IA2d: Achromatopsia (Congenital Stationary Cone Dysfunction)
IA2e: Blue Cone Monochromacy
IA2f: Congenital Stationary Night Blindness
IA2g: Congenital Stationary Synaptic Dysfunction
IB: Syndromic
II: Macular Diseases
III: Third Branch Disorders