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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
24
I: Photoreceptor Diseases
24
IA: Isolated
24
IA1: Acquired/Progressive
24
IA1a: Retinitis Pigmentosa
24
IA1ai: X-linked
IA1aii: Autosomal Dominant
24
SR58
| AD Retinitis Pigmentosa | Gene: RHO
SR68
| AD Retinitis Pigmentosa | Gene: RHO
SR143
| AD Retinitis Pigmentosa | Gene: RHO
SR182
| AD Retinitis Pigmentosa | Gene: RHO
SR1892
| AD Retinitis Pigmentosa | Gene: RHO
SR1987
| AD Retinitis Pigmentosa | Gene: RHO
SR2030
| AD Retinitis Pigmentosa | Gene: RHO
SR207
| AD Retinitis Pigmentosa | Gene: RHO
SR2393
| AD Retinitis Pigmentosa | Gene: RHO
SR2634
| AD Retinitis Pigmentosa | Gene: RHO
SR1063
| AD Retinitis Pigmentosa | Gene: PRPF31
SR539
| AD Retinitis Pigmentosa | Gene: PRPF31
SR717
| AD Retinitis Pigmentosa | Gene: PRPF31
SR980
| AD Retinitis Pigmentosa | Gene: PRPF31
SR1064
| AD Retinitis Pigmentosa | Gene: RP1
SR1297
| AD Retinitis Pigmentosa | Gene: RP1
SR1344
| AD Retinitis Pigmentosa | Gene: RP1
SR925
| AD Retinitis Pigmentosa | Gene: KLHL7
SR631
| AD Retinitis Pigmentosa | Gene: PRPF3
SR120
| AD Retinitis Pigmentosa | Gene: PRPF8
SR486
| AD Retinitis Pigmentosa | Gene: SNRNP200
SR3014
| AD Retinitis Pigmentosa | Gene: NRL
See More:
AD Retinitis Pigmentosa
Cases
SR549
| AD Retinitis Pigmentosa | Gene: RHO
SR651
| AD Retinitis Pigmentosa | Gene: RHO
IA1aiii: Autosomal Recessive
IA1b: Cone and Cone Rod Dystrophy
IA2: Congenital/Stationary
IA2a: LCA
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
IA2b: SECORD
IA2c: ECORD
IA2d: Achromatopsia (Congenital Stationary Cone Dysfunction)
IA2e: Blue Cone Monochromacy
IA2f: Congenital Stationary Night Blindness
IA2fi: X-linked CSNB
IA2fii: Autosomal Dominant
IA2fiii: Autosomal Recessive with Normal Fundus
IA2fiv: Enhanced S-cone Syndrome
SR1777
| Enhanced S-Cone Syndrome | Gene: NR2E3
SR28
| Enhanced S-Cone Syndrome | Gene: NR2E3
SR2134
| Enhanced S-Cone Syndrome | Gene: NR2E3
SR2295
| Enhanced S-Cone Syndrome | Gene: NR2E3
SR2720
| Enhanced S-Cone Syndrome | Gene: NR2E3
SR411
| Enhanced S-Cone Syndrome | Gene: NR2E3
SR67
| Enhanced S-Cone Syndrome | Gene: NR2E3
IA2fv: Fundus Albipunctatus
Other Congenital Stationary Night Blindness
IA2g: Congenital Stationary Synaptic Dysfunction
IB: Syndromic
II: Macular Diseases
IIA: Autosomal Recessive Stargardt Disease
IIB: Best Disease
IIC: Pattern Dystrophy
IID: Syndromic Macular Diseases
IIE: Occult Macular Dystrophy
IIF: Stargardt-like Dominant Macular Dystrophy
IIG: North Carolina Macular Dystrophy
IIH: Sorsby Fundus Dystrophy
SR23
| Sorsby Fundus Dystrophy | Gene: TIMP3
SR2273
| Sorsby Fundus Dystrophy | Gene: TIMP3
SR2290
| Sorsby Fundus Dystrophy | Gene: TIMP3
SR2324
| Sorsby Fundus Dystrophy | Gene: TIMP3
SR41
| Sorsby Fundus Dystrophy | Gene: TIMP3
IIJ: Malattia Leventinese
Other Macular Diseases
III: Third Branch Disorders