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QuickView for nyctalopia (phenotype)


Genetic Markers

Most Correlated Genes

Most Correlated SNPs

  1. SAG
  2. GRK1
  3. GRM6
  4. RHO
  5. CACNA1F
  1. No SNPs found
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Pathway Enrichment

Most Correlated Biogroups

  1. PID_RHODOPSIN_PATHWAY
  2. photoreceptor cell cilium
  3. 9+0 non-motile cilium
  4. response to light stimulus
  5. regulation of G-protein coupled receptor protein signaling pathway
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Curated Studies

Most Correlated Studies

  1. Mouse Phenotypes - Unspecified hereditary retinal dystrophies
  2. OMIM - Night blindness
  3. OMIM - Oguchi's disease
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Literature

Most Relevant Literature

  1. A MIDDLE-AGED PATIENT WITH BILATERAL VISION LOSS AND NYCTALOPIA.
  2. Onchocerciasis as a risk factor for night blindness.
  3. Birt-Hogg-Dubé syndrome associated with chorioretinopathy and nyctalopia: a case report and review o…
  4. Mutation analysis of pathogenic genes in a Henan family affected with congenital stationary night bl…
  5. Chromium and manganese levels in biological samples of normal and night blindness children of age gr…
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Clinical Trials

Most Relevant Clinical Trials

  1. Minocycline Treatment in Retinitis Pigmentosa
  2. Natural History Study of Patients With X-linked Retinal Dystrophy Associated With Mutations in Retin…
  3. A Patient Registry Study for Patients Treated With Voretigene Neparvovec in US
  4. Choroidal Thickness in Beta-thalassemia Patients
  5. Safety Study of Fenretinide in Adult Patients With Cystic Fibrosis
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