Inherited retinal dystrophy
MONDO:0019118An instance of retinal degeneration that is caused by an inherited modification of the individual's genome.
Also known as: fundus dystrophy, familial retinal dystrophy, genetic retinal dystrophy, hereditary retinal degeneration, hereditary retinal dystrophy, inherited retinal dystrophy, retinal dystrophy
524 clinical trials for this condition and its sub-types, 41 tagged with Inherited retinal dystrophy itself.
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Sub-types of Inherited retinal dystrophy
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Age-related macular degeneration 190 trials · 334 incl. sub-types
15 sub-types
- Wet macular degeneration 159 trials
- Dry age related macular degeneration 91 trials
- Age related macular degeneration 1 0 trials
- Age related macular degeneration 10 0 trials
- Age related macular degeneration 11 0 trials
- Age related macular degeneration 12 0 trials
- Age related macular degeneration 14 0 trials
- Age related macular degeneration 2 0 trials
- Age related macular degeneration 4 0 trials
- Age related macular degeneration 6 0 trials
- Age related macular degeneration 7 0 trials
- Age related macular degeneration 8 0 trials
- Age related macular degeneration 9 0 trials
- Macular degeneration, age-related, 3 0 trials
- Macular dystrophy with central cone involvement 0 trials
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Retinitis pigmentosa 84 trials · 89 incl. sub-types
101 sub-types
- Retinitis pigmentosa 3 7 trials
- Retinitis pigmentosa 4 5 trials
- Retinitis pigmentosa 11 4 trials
- Retinitis pigmentosa 39 3 trials
- Retinitis pigmentosa 1 1 trial
- Retinitis pigmentosa 25 1 trial
- Retinitis pigmentosa 37 1 trial
- Retinitis pigmentosa 40 1 trial
- Retinitis pigmentosa 45 1 trial
- Retinitis pigmentosa 47 1 trial
- Retinitis pigmentosa Y-linked 1 trial
- Autosomal recessive pericentral pigmentary retinopathy 0 trials
- Cone-rod dystrophy 15 0 trials
- Cone-rod dystrophy 16 0 trials
- Cone-rod dystrophy 2 0 trials
- Dominant pericentral pigmentary retinopathy 0 trials
- Late-adult onset retinitis pigmentosa 0 trials
- Retinal dystrophy and obesity 0 trials
- Retinitis pigmentosa 10 0 trials
- Retinitis pigmentosa 100 0 trials
- Retinitis pigmentosa 12 0 trials
- Retinitis pigmentosa 13 0 trials
- Retinitis pigmentosa 14 0 trials
- Retinitis pigmentosa 17 0 trials
- Retinitis pigmentosa 18 0 trials
- Retinitis pigmentosa 19 0 trials
- Retinitis pigmentosa 2 0 trials
- Retinitis pigmentosa 20 0 trials
- Retinitis pigmentosa 22 0 trials
- Retinitis pigmentosa 23 0 trials
- Retinitis pigmentosa 24 0 trials
- Retinitis pigmentosa 26 0 trials
- Retinitis pigmentosa 27 0 trials
- Retinitis pigmentosa 28 0 trials
- Retinitis pigmentosa 29 0 trials
- Retinitis pigmentosa 30 0 trials
- Retinitis pigmentosa 31 0 trials
- Retinitis pigmentosa 32 0 trials
- Retinitis pigmentosa 33 0 trials
- Retinitis pigmentosa 34 0 trials
- Retinitis pigmentosa 35 0 trials
- Retinitis pigmentosa 36 0 trials
- Retinitis pigmentosa 38 0 trials
- Retinitis pigmentosa 41 0 trials
- Retinitis pigmentosa 42 0 trials
- Retinitis pigmentosa 43 0 trials
- Retinitis pigmentosa 44 0 trials
- Retinitis pigmentosa 46 0 trials
- Retinitis pigmentosa 48 0 trials
- Retinitis pigmentosa 49 0 trials
- Retinitis pigmentosa 50 0 trials
- Retinitis pigmentosa 51 0 trials
- Retinitis pigmentosa 53 0 trials
- Retinitis pigmentosa 54 0 trials
- Retinitis pigmentosa 55 0 trials
- Retinitis pigmentosa 56 0 trials
- Retinitis pigmentosa 57 0 trials
- Retinitis pigmentosa 58 0 trials
- Retinitis pigmentosa 59 0 trials
- Retinitis pigmentosa 6 0 trials
- Retinitis pigmentosa 60 0 trials
- Retinitis pigmentosa 61 0 trials
- Retinitis pigmentosa 62 0 trials
- Retinitis pigmentosa 63 0 trials
- Retinitis pigmentosa 64 0 trials
- Retinitis pigmentosa 65 0 trials
- Retinitis pigmentosa 66 0 trials
- Retinitis pigmentosa 67 0 trials
- Retinitis pigmentosa 68 0 trials
- Retinitis pigmentosa 69 0 trials
- Retinitis pigmentosa 7 0 trials
- Retinitis pigmentosa 7, digenic 0 trials
- Retinitis pigmentosa 70 0 trials
- Retinitis pigmentosa 71 0 trials
- Retinitis pigmentosa 72 0 trials
- Retinitis pigmentosa 73 0 trials
- Retinitis pigmentosa 74 0 trials
- Retinitis pigmentosa 75 0 trials
- Retinitis pigmentosa 76 0 trials
- Retinitis pigmentosa 77 0 trials
- Retinitis pigmentosa 78 0 trials
- Retinitis pigmentosa 79 0 trials
- Retinitis pigmentosa 80 0 trials
- Retinitis pigmentosa 81 0 trials
- Retinitis pigmentosa 83 0 trials
- Retinitis pigmentosa 84 0 trials
- Retinitis pigmentosa 85 0 trials
- Retinitis pigmentosa 86 0 trials
- Retinitis pigmentosa 87 with choroidal involvement 0 trials
- Retinitis pigmentosa 88 0 trials
- Retinitis pigmentosa 9 0 trials
- Retinitis pigmentosa 90 0 trials
- Retinitis pigmentosa 92 0 trials
- Retinitis pigmentosa 93 0 trials
- Retinitis pigmentosa 94, variable age at onset 0 trials
- Retinitis pigmentosa 95 0 trials
- Retinitis pigmentosa 96 0 trials
- Retinitis pigmentosa 97 0 trials
- Retinitis pigmentosa 98 0 trials
- Retinitis pigmentosa 99 0 trials
- Retinitis pigmentosa with or without situs inversus 0 trials
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Hereditary macular dystrophy 3 trials · 72 incl. sub-types
17 sub-types
- Familial flecked retinopathy 0 trials · 45 incl. sub-types Sub-types →
- Macular corneal dystrophy 13 trials
- Vitelliform macular dystrophy 6 trials · 10 incl. sub-types Sub-types →
- Cone dystrophy 4 trials Sub-types →
- AICA-ribosiduria 1 trial
- Macular dystrophy, retinal 1 trial Sub-types →
- EEM syndrome 0 trials
- Benign concentric annular macular dystrophy 0 trials
- Coloboma of macula 0 trials
- Coloboma of macula-brachydactyly type B syndrome 0 trials
- Macular coloboma-cleft palate-hallux valgus syndrome 0 trials
- Macular dystrophy with or without cone dysfunction 0 trials
- Macular dystrophy, X-linked 0 trials
- Macular dystrophy, fenestrated sheen type 0 trials
- Occult macular dystrophy 0 trials
- Patterned dystrophy of the retinal pigment epithelium 0 trials Sub-types →
- Renal hypomagnesemia 5 with ocular involvement 0 trials
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Cone-rod dystrophy 17 trials · 21 incl. sub-types
28 sub-types
- X-linked cone-rod dystrophy 0 trials · 2 incl. sub-types Sub-types →
- Cone-rod dystrophy 10 1 trial
- Cone-rod dystrophy 6 1 trial
- Leber congenital amaurosis 4 0 trials
- Newfoundland cone-rod dystrophy 0 trials
- Cone dystrophy 3 0 trials
- Cone-rod dystrophy 1 0 trials
- Cone-rod dystrophy 11 0 trials
- Cone-rod dystrophy 12 0 trials
- Cone-rod dystrophy 13 0 trials
- Cone-rod dystrophy 14 0 trials
- Cone-rod dystrophy 15 0 trials
- Cone-rod dystrophy 16 0 trials
- Cone-rod dystrophy 17 0 trials
- Cone-rod dystrophy 18 0 trials
- Cone-rod dystrophy 19 0 trials
- Cone-rod dystrophy 2 0 trials
- Cone-rod dystrophy 20 0 trials
- Cone-rod dystrophy 21 0 trials
- Cone-rod dystrophy 22 0 trials
- Cone-rod dystrophy 24 0 trials
- Cone-rod dystrophy 3 0 trials
- Cone-rod dystrophy 5 0 trials
- Cone-rod dystrophy 7 0 trials
- Cone-rod dystrophy 8 0 trials
- Cone-rod dystrophy 9 0 trials
- Macular degeneration, X-linked atrophic 0 trials
- Retinal cone dystrophy 4 0 trials
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Leber congenital amaurosis 11 trials · 13 incl. sub-types
21 sub-types
- Leber congenital amaurosis 2 3 trials
- Leber congenital amaurosis 10 2 trials
- Leber congenital amaurosis 5 2 trials
- Leber congenital amaurosis 1 1 trial
- Leber congenital amaurosis 11 0 trials
- Leber congenital amaurosis 12 0 trials
- Leber congenital amaurosis 13 0 trials
- Leber congenital amaurosis 14 0 trials
- Leber congenital amaurosis 15 0 trials
- Leber congenital amaurosis 16 0 trials
- Leber congenital amaurosis 17 0 trials
- Leber congenital amaurosis 18 0 trials
- Leber congenital amaurosis 19 0 trials
- Leber congenital amaurosis 3 0 trials
- Leber congenital amaurosis 4 0 trials
- Leber congenital amaurosis 6 0 trials
- Leber congenital amaurosis 7 0 trials
- Leber congenital amaurosis 8 0 trials
- Leber congenital amaurosis 9 0 trials
- Leber congenital amaurosis with early-onset deafness 0 trials
- Retinal aplasia 0 trials
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ABCA4-related retinopathy 7 trials · 13 incl. sub-types
3 sub-types
- Severe early-childhood-onset retinal dystrophy 10 trials
- Cone-rod dystrophy 3 0 trials
- Retinitis pigmentosa 19 0 trials
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RPE65-related recessive retinopathy 5 trials · 8 incl. sub-types
2 sub-types
- Leber congenital amaurosis 2 3 trials
- Retinitis pigmentosa 20 0 trials
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BEST1-related dominant retinopathy 1 trial · 7 incl. sub-types
1 sub-type
- Vitelliform macular dystrophy 2 7 trials
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RHO-related retinopathy 0 trials · 7 incl. sub-types
2 sub-types
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RPGR-related retinopathy 0 trials · 7 incl. sub-types
3 sub-types
- Retinitis pigmentosa 3 7 trials
- X-linked cone-rod dystrophy 1 0 trials
- Macular degeneration, X-linked atrophic 0 trials
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Choroideremia 6 trials
2 sub-types
- Choroideremia hypopituitarism 0 trials
- Total central choroidal atrophy 0 trials
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X-linked retinoschisis 4 trials
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PRPF31-related retinopathy 1 trial · 4 incl. sub-types
1 sub-type
- Retinitis pigmentosa 11 4 trials
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RLBP1-related retinopathy 2 trials · 3 incl. sub-types
3 sub-types
- Fundus albipunctatus 1 trial Sub-types →
- Bothnia retinal dystrophy 0 trials
- Newfoundland cone-rod dystrophy 0 trials
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ELOVL4-related maculopathy 0 trials · 3 incl. sub-types
1 sub-type
- Stargardt disease 3 3 trials
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Revesz syndrome 2 trials
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Late-onset retinal degeneration 2 trials
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EYS-related retinopathy 1 trial · 2 incl. sub-types
1 sub-type
- Retinitis pigmentosa 25 1 trial
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LCA5-related retinopathy 1 trial · 2 incl. sub-types
1 sub-type
- Leber congenital amaurosis 5 2 trials
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PRPH2-related retinopathy 1 trial · 2 incl. sub-types
7 sub-types
- Fundus albipunctatus 1 trial Sub-types →
- Leber congenital amaurosis 18 0 trials
- Choroidal dystrophy, central areolar 2 0 trials
- Patterned macular dystrophy 1 0 trials
- Retinitis pigmentosa 7 0 trials
- Retinitis pigmentosa 7, digenic 0 trials
- Vitelliform macular dystrophy 3 0 trials
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BEST1-related recessive retinopathy 0 trials · 2 incl. sub-types
1 sub-type
- Autosomal recessive bestrophinopathy 2 trials
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AIPL1-related retinopathy 1 trial
1 sub-type
- Leber congenital amaurosis 4 0 trials
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Retinoschisis of fovea 1 trial
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ATF6-related retinopathy 0 trials · 1 incl. sub-types
1 sub-type
- Achromatopsia 7 1 trial
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CNGB1-related retinopathy 0 trials · 1 incl. sub-types
1 sub-type
- Retinitis pigmentosa 45 1 trial
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FLVCR1-related retinopathy with or without ataxia 0 trials · 1 incl. sub-types
1 sub-type
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GUCY2D retinopathy 0 trials · 1 incl. sub-types
3 sub-types
- GUCY2D-related recessive retinopathy 0 trials · 1 incl. sub-types Sub-types →
- Cone-rod dystrophy 6 1 trial
- GUCY2D-related dominant retinopathy 0 trials Sub-types →
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RDH5-related retinopathy 0 trials · 1 incl. sub-types
1 sub-type
- Fundus albipunctatus 1 trial Sub-types →
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ADAM9-related retinopathy 0 trials
1 sub-type
- Cone-rod dystrophy 9 0 trials
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CACNA1F-related retinopathy 0 trials
3 sub-types
- Aland island eye disease 0 trials
- X-linked cone-rod dystrophy 3 0 trials
- Congenital stationary night blindness 2A 0 trials
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CACNA2D4-related retinopathy 0 trials
1 sub-type
- Retinal cone dystrophy 4 0 trials
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CDHR1-related retinopathy 0 trials
3 sub-types
- Cone-rod dystrophy 15 0 trials
- Macular dystrophy, retinal, 5 0 trials
- Retinitis pigmentosa 65 0 trials
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CERKL-related retinopathy 0 trials
1 sub-type
- Retinitis pigmentosa 26 0 trials
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CNGA1-related retinopathy 0 trials
1 sub-type
- Retinitis pigmentosa 49 0 trials
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CNGA3-related retinopathy 0 trials
1 sub-type
- Achromatopsia 2 0 trials
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CRX-related retinopathy 0 trials
2 sub-types
- Leber congenital amaurosis 7 0 trials
- Cone-rod dystrophy 2 0 trials
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GNAT2-related retinopathy 0 trials
1 sub-type
- Achromatopsia 4 0 trials
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GPR179-related retinopathy 0 trials
1 sub-type
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GRM6-related retinopathy 0 trials
1 sub-type
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GUCA1A-related retinopathy 0 trials
2 sub-types
- Cone dystrophy 3 0 trials
- Cone-rod dystrophy 14 0 trials
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HGSNAT-related retinopathy 0 trials
1 sub-type
- Retinitis pigmentosa 73 0 trials
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IDH3B-related retinopathy 0 trials
1 sub-type
- Retinitis pigmentosa 46 0 trials
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IMPDH1-related retinopathy 0 trials
2 sub-types
- Leber congenital amaurosis 11 0 trials
- Retinitis pigmentosa 10 0 trials
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IMPG1-related dominant retinopathy 0 trials
1 sub-type
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IMPG1-related recessive retinopathy 0 trials
1 sub-type
- Vitelliform macular dystrophy 4 0 trials
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IMPG2-related dominant retinopathy 0 trials
1 sub-type
- Vitelliform macular dystrophy 5 0 trials
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IMPG2-related recessive retinopathy 0 trials
1 sub-type
- Retinitis pigmentosa 56 0 trials
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KCNV2-related retinopathy 0 trials
1 sub-type
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KIZ-related retinopathy 0 trials
1 sub-type
- Retinitis pigmentosa 69 0 trials
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LRIT3-related retinopathy 0 trials
1 sub-type
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MAK-related retinopathy 0 trials
1 sub-type
- Retinitis pigmentosa 62 0 trials
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MERTK-related retinopathy 0 trials
1 sub-type
- Retinitis pigmentosa 38 0 trials
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MRCS syndrome 0 trials
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NMNAT1-related retinopathy 0 trials
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NYX-related retinopathy 0 trials
1 sub-type
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Oguchi disease 0 trials
2 sub-types
- Oguchi disease-1 0 trials
- Oguchi disease-2 0 trials
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PCARE-related retinopathy 0 trials
1 sub-type
- Retinitis pigmentosa 54 0 trials
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PDE6A-related retinopathy 0 trials
1 sub-type
- Retinitis pigmentosa 43 0 trials
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PDE6C-related retinopathy 0 trials
1 sub-type
- Cone dystrophy 4 0 trials Sub-types →
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PDE6G-related retinopathy 0 trials
1 sub-type
- Retinitis pigmentosa 57 0 trials
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PROM1-related retinopathy 0 trials
3 sub-types
- PROM1-related dominant retinopathy 0 trials Sub-types →
- PROM1-related recessive retinopathy 0 trials Sub-types →
- Cone-rod dystrophy 12 0 trials
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PRPF8-related retinopathy 0 trials
1 sub-type
- Retinitis pigmentosa 13 0 trials
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RAB28-related retinopathy 0 trials
1 sub-type
- Cone-rod dystrophy 18 0 trials
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RD3-related retinopathy 0 trials
1 sub-type
- Leber congenital amaurosis 12 0 trials
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RDH12-related dominant retinopathy 0 trials
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RDH12-related recessive retinopathy 0 trials
1 sub-type
- Leber congenital amaurosis 13 0 trials
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REEP6-related retinopathy 0 trials
1 sub-type
- Retinitis pigmentosa 77 0 trials
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RP1-related dominant retinopathy 0 trials
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RP1-related recessive retinopathy 0 trials
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RP2-related retinopathy 0 trials
1 sub-type
- Retinitis pigmentosa 2 0 trials
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RPE65-related dominant retinopathy 0 trials
1 sub-type
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1 sub-type
- Retinitis pigmentosa 33 0 trials
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SPATA7-related retinopathy 0 trials
2 sub-types
- Leber congenital amaurosis 3 0 trials
- Retinitis pigmentosa 94, variable age at onset 0 trials
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Sorsby fundus dystrophy 0 trials
1 sub-type
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TOPORS-related retinopathy 0 trials
1 sub-type
- Retinitis pigmentosa 31 0 trials
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TRPM1-related retinopathy 0 trials
1 sub-type
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TTLL5-related retinopathy 0 trials
1 sub-type
- Cone-rod dystrophy 19 0 trials
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X-linked retinal dysplasia 0 trials
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Aceruloplasminemia 0 trials
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Amaurosis-hypertrichosis syndrome 0 trials
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Familial benign flecked retina 0 trials
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Macular degeneration, early-onset 0 trials
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Microcephaly and chorioretinopathy 1 0 trials
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Oligocone trichromacy 0 trials
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1 sub-type
- Basal laminar drusen 0 trials
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Retinoschisis, autosomal dominant 0 trials
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Vitreoretinal dystrophy 0 trials
Most studied deeper sub-types
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Could a common diabetes drug protect eyesight in stargardt disease?
Disease control OngoingThis study tests whether metformin, a widely used diabetes drug, can safely slow vision loss in people with ABCA4 retinopathy (Stargardt disease). Fifty-five participants aged 12 and older will take metformin by mouth for 24 months, with regular eye exams to track changes. The go…
Phase 1/2 • Sponsor: National Eye Institute (NEI) • Aim: Disease control
Last updated Aug 21, 2026 00:00 UTC
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Experimental eye drug shows promise for rare Blindness-Causing disease
Disease control OngoingThis study tests an experimental drug called VP-001 for people with a rare genetic eye disease that causes vision loss. The drug is injected into the eye and aims to slow or stop further damage. Researchers will check safety and measure any changes in eyesight over about two year…
Phase 1/2 • Sponsor: PYC Therapeutics • Aim: Disease control
Last updated Jun 27, 2026 13:00 UTC
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One-Time eye injection could slow blindness in retinitis pigmentosa
Disease control OngoingThis study tests a gene therapy called SPVN06 for retinitis pigmentosa, an inherited eye disease that causes gradual vision loss. The treatment is given as a single injection under the retina. The trial includes 33 adults with advanced disease and will check safety and whether it…
Phase 1/2 • Sponsor: SparingVision • Aim: Disease control
Last updated Jun 27, 2026 12:33 UTC
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Gene therapy injection aims to halt blindness from rare eye disorder
Disease control OngoingThis Phase 3 trial tests a gene therapy called VGR-R01 for Bietti crystalline dystrophy, a rare inherited condition that leads to progressive vision loss. The study will enroll 45 adults who receive either the gene therapy injection under the retina or a control treatment. Resear…
Phase 3 • Sponsor: Shanghai Vitalgen BioPharma Co., Ltd. • Aim: Disease control
Last updated Jun 27, 2026 08:07 UTC
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Custom drug targets rare blindness in One-Patient trial
Disease control OngoingThis study tests a custom-made drug called an antisense oligonucleotide, designed specifically for one person with retinal dystrophy caused by a PRPH2 gene mutation. The drug aims to correct the genetic error and potentially slow vision loss. The trial involves only one participa…
Phase 1/2 • Sponsor: n-Lorem Foundation • Aim: Disease control
Last updated Jun 26, 2026 17:51 UTC
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Sound-Guided gaze: new device aims to sharpen eye imaging for the visually impaired
Symptom relief By invitation onlyThis study tests a device that uses real-time sound feedback to help people with vision loss fix their gaze on a target. Participants hear sounds that guide their eyes back to center when they drift. The goal is to improve the quality of eye imaging by reducing blur from eye move…
Sponsor: University Medical Center Goettingen • Aim: Symptom relief
Last updated Jun 27, 2026 12:08 UTC
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New eye tests could speed up retinitis pigmentosa treatment trials
Knowledge-focused OngoingThis study aims to find better ways to measure how retinitis pigmentosa (a genetic eye disease that causes vision loss) progresses over time. Researchers will use advanced imaging and vision tests in 40 people with specific genetic forms of the disease. The goal is to identify re…
Sponsor: University Hospital Tuebingen • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:29 UTC
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Scientists track vision loss in rare genetic eye disease to pave way for future treatments
Knowledge-focused OngoingThis study follows 50 people with a rare inherited eye condition called PRPF31-related retinal dystrophy (RP11) to see how their vision changes over time. Researchers will measure things like visual acuity, retinal thickness, and quality of life using eye exams and questionnaires…
Sponsor: PYC Therapeutics • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:07 UTC