StoneRounds
Volunteer
Un-volunteer
Open Diagnosis Box
Leaderboard
StoneRounds
Disease Atlas
SR:
Volunteer
Un-volunteer
Open Diagnosis Box
Leaderboard
Search
Not logged in
Log in
Register
Terms of Use
Join Teaching Session
Log in
Register
Terms of Use
Join Teaching Session
Search
StoneRounds
Disease Atlas
JavaScript is disabled.
Without JavaScript enabled, this site will not function properly.
Please follow
these instructions
in order to enable JavaScript in your browser.
Disease Atlas
Search
Reset
Create
Show Cases Added By Recency:
All Time
Last Month
Last Six Months
Last Year
Expand all
/
Collapse all
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
SR869
| Occult Macular Dystrophy | Gene: RP1L1
SR1887
| Occult Macular Dystrophy | Gene: RP1L1
SR879
| Occult Macular Dystrophy | Gene: RP1L1
SR955
| Occult Macular Dystrophy | Gene: RP1L1
SR988
| Occult Macular Dystrophy | Gene: RP1L1
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