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Up to: Hereditary neurological disease · Perceptual disorders · Retinal degeneration

Inherited retinal dystrophy

An instance of retinal degeneration that is caused by an inherited modification of the individual's genome.

41 trials tagged with this condition →

Age-related macular degeneration 190 trials · 334 incl. sub-types Sub-types →
Retinitis pigmentosa 84 trials · 89 incl. sub-types Sub-types →
Hereditary macular dystrophy 3 trials · 70 incl. sub-types Sub-types →
Cone-rod dystrophy 17 trials · 21 incl. sub-types Sub-types →
Leber congenital amaurosis 10 trials · 12 incl. sub-types Sub-types →
ABCA4-related retinopathy 7 trials · 11 incl. sub-types Sub-types →
RPE65-related recessive retinopathy 5 trials · 7 incl. sub-types Sub-types →
BEST1-related dominant retinopathy 1 trial · 7 incl. sub-types Sub-types →
RHO-related retinopathy 0 trials · 7 incl. sub-types Sub-types →
RPGR-related retinopathy 0 trials · 7 incl. sub-types Sub-types →
Choroideremia 6 trials Sub-types →
X-linked retinoschisis 4 trials
Ornithine aminotransferase deficiency 4 trials
PRPF31-related retinopathy 1 trial · 4 incl. sub-types Sub-types →
Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations 3 trials
RLBP1-related retinopathy 2 trials · 3 incl. sub-types Sub-types →
ELOVL4-related maculopathy 0 trials · 3 incl. sub-types Sub-types →
Revesz syndrome 2 trials
Late-onset retinal degeneration 2 trials
EYS-related retinopathy 1 trial · 2 incl. sub-types Sub-types →
LCA5-related retinopathy 1 trial · 2 incl. sub-types Sub-types →
PRPH2-related retinopathy 1 trial · 2 incl. sub-types Sub-types →
BEST1-related recessive retinopathy 0 trials · 2 incl. sub-types Sub-types →
AIPL1-related retinopathy 1 trial Sub-types →
Retinoschisis of fovea 1 trial
ATF6-related retinopathy 0 trials · 1 incl. sub-types Sub-types →
CNGB1-related retinopathy 0 trials · 1 incl. sub-types Sub-types →
FLVCR1-related retinopathy with or without ataxia 0 trials · 1 incl. sub-types Sub-types →
GUCY2D retinopathy 0 trials · 1 incl. sub-types Sub-types →
RDH5-related retinopathy 0 trials · 1 incl. sub-types Sub-types →
ADAM9-related retinopathy 0 trials Sub-types →
CACNA1F-related retinopathy 0 trials Sub-types →
CACNA2D4-related retinopathy 0 trials Sub-types →
CDHR1-related retinopathy 0 trials Sub-types →
CERKL-related retinopathy 0 trials Sub-types →
CNGA1-related retinopathy 0 trials Sub-types →
CNGA3-related retinopathy 0 trials Sub-types →
CRX-related retinopathy 0 trials Sub-types →
GNAT2-related retinopathy 0 trials Sub-types →
GPR179-related retinopathy 0 trials Sub-types →
GRM6-related retinopathy 0 trials Sub-types →
GUCA1A-related retinopathy 0 trials Sub-types →
HGSNAT-related retinopathy 0 trials Sub-types →
IDH3B-related retinopathy 0 trials Sub-types →
IMPDH1-related retinopathy 0 trials Sub-types →
IMPG1-related dominant retinopathy 0 trials Sub-types →
IMPG1-related recessive retinopathy 0 trials Sub-types →
IMPG2-related dominant retinopathy 0 trials Sub-types →
IMPG2-related recessive retinopathy 0 trials Sub-types →
KCNV2-related retinopathy 0 trials Sub-types →
KIZ-related retinopathy 0 trials Sub-types →
LRIT3-related retinopathy 0 trials Sub-types →
MAK-related retinopathy 0 trials Sub-types →
MERTK-related retinopathy 0 trials Sub-types →
MRCS syndrome 0 trials
NMNAT1-related retinopathy 0 trials Sub-types →
NYX-related retinopathy 0 trials Sub-types →
Oguchi disease 0 trials Sub-types →
PCARE-related retinopathy 0 trials Sub-types →
PDE6A-related retinopathy 0 trials Sub-types →
PDE6C-related retinopathy 0 trials Sub-types →
PDE6G-related retinopathy 0 trials Sub-types →
PROM1-related retinopathy 0 trials Sub-types →
PRPF8-related retinopathy 0 trials Sub-types →
RAB28-related retinopathy 0 trials Sub-types →
RD3-related retinopathy 0 trials Sub-types →
RDH12-related dominant retinopathy 0 trials
RDH12-related recessive retinopathy 0 trials Sub-types →
REEP6-related retinopathy 0 trials Sub-types →
RP1-related dominant retinopathy 0 trials
RP1-related recessive retinopathy 0 trials
RP2-related retinopathy 0 trials Sub-types →
RPE65-related dominant retinopathy 0 trials Sub-types →
SNRNP200-related dominant retinopathy 0 trials Sub-types →
SPATA7-related retinopathy 0 trials Sub-types →
Sorsby fundus dystrophy 0 trials Sub-types →
TOPORS-related retinopathy 0 trials Sub-types →
TRPM1-related retinopathy 0 trials Sub-types →
TTLL5-related retinopathy 0 trials Sub-types →
X-linked intellectual disability-limb spasticity-retinal dystrophy-diabetes insipidus syndrome 0 trials
X-linked retinal dysplasia 0 trials
Aceruloplasminemia 0 trials
Amaurosis-hypertrichosis syndrome 0 trials
Choroideremia-deafness-obesity syndrome 0 trials
Dystrophies primarily involving the retinal pigment epithelium 0 trials
Ectopia lentis-chorioretinal dystrophy-myopia syndrome 0 trials
Familial benign flecked retina 0 trials
Foveal hypoplasia-presenile cataract syndrome 0 trials
Helicoid peripapillary chorioretinal degeneration 0 trials
Infantile cerebellar-retinal degeneration 0 trials
Macular degeneration, early-onset 0 trials
Microcephaly and chorioretinopathy 1 0 trials
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability 0 trials
Microcornea-myopic chorioretinal atrophy 0 trials
Oligocone trichromacy 0 trials
Pigmented paravenous retinochoroidal atrophy 0 trials
Progressive bifocal chorioretinal atrophy 0 trials
Progressive retinal dystrophy due to retinol transport defect 0 trials
Retinal degeneration-nanophthalmos-glaucoma syndrome 0 trials
Retinal dystrophies primarily involving Bruch's membrane 0 trials Sub-types →
Retinal dystrophy in systemic or cerebroretinal lipidoses 0 trials
Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies 0 trials
Retinal dystrophy, X-linked, Gardner-Hardcastle type 0 trials
Retinoschisis, autosomal dominant 0 trials
Vitreoretinal dystrophy 0 trials