Myopia 25, autosomal dominant

Summary

Myopia, or nearsightedness, is a refractive error of the eye. Light rays from a distant object are focused in front of the retina and those from a near object are focused in the retina; therefore distant objects are blurry and near objects are clear (summary by Kaiser et al., 2004). For a discussion of genetic heterogeneity of susceptibility to myopia, see 160700. [from OMIM]

Available tests

6 tests are in the database for this condition.

Clinical tests (6 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

P4HA2
9 tests
Also known as: MYP25, lncRNA-PE, P4HA2
Summary: prolyl 4-hydroxylase subunit alpha 2

Imported from Human Phenotype Ontology (HPO)

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Abnormality of the eye
- High myopia
  High myopia
  - MedGen UID: 78759
  - Concept ID: C0271183
  - Finding: Disease or Syndrome
  Abnormality of the eye
  See: Feature record | Search on this feature
- Retinal detachment
  Retinal detachment
  - MedGen UID: 19759
  - Concept ID: C0035305
  - Finding: Disease or Syndrome
  Abnormality of the eye
  See: Feature record | Search on this feature

Reviews

Clinical resources

Molecular resources

Consumer resources

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