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GTR Home > Conditions/Phenotypes > EDICT syndrome

EDICT syndrome

Synonyms
ENDOTHELIAL DYSTROPHY, IRIS HYPOPLASIA, CONGENITAL CATARACT, AND STROMAL THINNING SYNDROME; KERATOCONUS WITH CATARACT; KERATOCONUS, FAMILIAL, WITH EARLY-ONSET ANTERIOR POLAR CATARACT
Modes of inheritance
Autosomal dominant inheritance (Orphanet)

Summary

EDICT syndrome is an autosomal dominant syndromal anterior segment dysgenesis characterized by endothelial dystrophy, iris hypoplasia, congenital cataract, and thinning of the corneal stroma (Iliff et al., 2012). Syndromes with overlapping features have been reported, including cornea guttata with anterior polar cataracts (121390) and congenital corneal opacities, cornea guttata, and corectopia (608484). [from OMIM]

Available tests

8 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (8 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: EDICT, MIRN184, miR-184, MIR184
    Summary: microRNA 184

Clinical features

Help
Imported from Human Phenotype Ontology (HPO)

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