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GTR Home > Conditions/Phenotypes > Keratoconus 9

Keratoconus 9

Summary

Keratoconus-9 (KTCN9), a degenerative corneal disease with onset during adolescence, is characterized by corneal ectasia, thinning, and cone-shaped protrusion that results in reduced vision (Hao et al., 2017). For a discussion of genetic heterogeneity of keratoconus, see 148300. [from OMIM]

Available tests

2 tests are in the database for this condition.

Clinical tests (2 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: H2-ALPHA, KTCN9, TUBA2, TUBA3D
    Summary: tubulin alpha 3d

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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