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(e.g. rs3825942, FOXP1, Response to oxidative stress, Ischemia, Hypothalamus, Quercetin)
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QuickView for anophthalmia (phenotype)


Genetic Markers

Most Correlated Genes

Most Correlated SNPs

  1. FRAS1
  2. FREM2
  1. No SNPs found
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Pathway Enrichment

Most Correlated Biogroups

  1. CSPG repeat
  2. Na-Ca exchanger/integrin-beta4
  3. CalX-like domain superfamily
  4. basement membrane
  5. collagen-containing extracellular matrix
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Curated Studies

Most Correlated Studies

  1. Mouse Phenotypes - Congenital abnormality
  2. OMIM - Congenital disorder
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Literature

Most Relevant Literature

  1. Clinical and genetic analysis further delineates the phenotypic spectrum of ALDH1A3-related anophtha…
  2. Stepwise self-inflating hydrogel expansion for congenital anophthalmia and blind microphthalmia: Ove…
  3. Unusual onset of Graves' disease associated with thymic hyperplasia in a 5-year-old girl with congen…
  4. Identification of novel homozygous variants in FOXE3 and AP4M1 underlying congenital syndromic anoph…
  5. Holoprosencephaly with a Special Form of Anophthalmia Result from Experimental Induction of bmp4, Ov…
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Clinical Trials

Most Relevant Clinical Trials

  1. Molecular Analysis of Microphthalmia/Anophthalmia
  2. Microphthalmia, Anophthalmia, and Coloboma Genetic Epidemiology in Children
  3. Pathogenesis and Genetics of Microphthalmia, Anophthalmia and Uveal Coloboma (MAC)
  4. Quality of Life in Children Glaucoma and Cataract
  5. Subjective Perception of Ocular Prosthesis Wear
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