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Rod dystrophy
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
No genes found
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
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Curated Studies
Most Correlated Studies
Mouse Phenotypes - Unspecified hereditary retinal dystrophies
OMIM - Retinal dystrophy
OMIM - Spondylometaphyseal dysplasia
OMIM - Progressive cone-rod dystrophy
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Literature
Most Relevant Literature
Coexistence of KCNV2 associated cone dystrophy with supernormal rod electroretinogram and MFRP relat…
Cone dystrophy with supranormal rod response' in children.
Restoration of vision in the pde6β-deficient dog, a large animal model of rod-cone dystrophy.
Mutation screening of the GUCA1B gene in patients with autosomal dominant cone and cone rod dystroph…
Novel mutations in MERTK associated with childhood onset rod-cone dystrophy.
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Clinical Trials
Most Relevant Clinical Trials
Phenotype Correlates Genotype of Inherited Retina Dystrophies, Retinitis Pigmentosa, Con>Rod Dystrop…
Promising ROd-cone DYstrophy Gene therapY
Interferon Gamma-1b Administered Topically for Macular Edema/Intraretinal Schisis Cysts in Rod-Cone …
Heart Imaging in Children With Muscular Dystrophy
Compensation for Blindness With the Intelligent Retinal Implant System (IRIS V2) in Patients With Re…
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