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QuickView for retinoschisis (phenotype)


Genetic Markers

Most Correlated Genes

Most Correlated SNPs

  1. RS1
  1. No SNPs found
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Pathway Enrichment

Most Correlated Biogroups

  1. light adaption
  2. Coagulation factor 5/8 C-terminal domain
  3. MODULE_287
  4. detection of light stimulus
  5. Galactose-binding-like domain superfamily
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Curated Studies

Most Correlated Studies

  1. Mouse Phenotypes - Unspecified hereditary retinal dystrophies
  2. OMIM - Retinal degeneration
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Literature

Most Relevant Literature

  1. The genetic spectrum and clinical features of X-linked juvenile retinoschisis in Central China.
  2. Retinal Folds as a Clinical Feature of X-Linked Retinoschisis: A Series of Three Cases.
  3. Vitreous Hemorrhage in Pediatric Patients With X-Linked Retinoschisis: Characteristics and Outcomes.
  4. X-Linked Retinoschisis: Deep Phenotyping and Genetic Characterization.
  5. STELLATE NONHEREDITARY IDIOPATHIC FOVEOMACULAR RETINOSCHISIS: NOVEL FINDINGS AND OPTICAL COHERENCE T…
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Clinical Trials

Most Relevant Clinical Trials

  1. Optical Coherence Tomography Evaluation of Retinoschisis and Retinal Detachment
  2. Macular Retinoschisis and Detachment Associated With Glaucomatous Optic Neuropathy
  3. Macular Tractional Retinoschisis in Proliferative Diabetic Retinopathy
  4. Clinical and Genetic Studies of X-Linked Juvenile Retinoschisis
  5. Study of RS1 Ocular Gene Transfer for X-linked Retinoschisis
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