Edict Syndrome (EDICT)

Alias:

Ktcnct

Endothelial Dystrophy, Iris Hypoplasia, Congenital Cataract, and Stromal Thinning Syndrome

Endothelial Dystrophy-Iris Hypoplasia-Congenital Cataract-Stromal Thinning Syndrome

Autosomal Dominant Keratoconus with Early-Onset Anterior Polar Cataracts

Keratoconus, Familial, with Early-Onset Anterior Polar Cataract

Familial Keratoconus with Cataract

Keratoconus with Cataract

Edict

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Edict Syndrome, also known as ktcnct, is related to keratoconus and corneal endothelial dystrophy. An important gene associated with Edict Syndrome is MIR184 (MicroRNA 184). Affiliated tissues include endothelial and eye, and related phenotypes are keratoconus and astigmatism

Related ID：

MALACARDS：EDC001

OMIM：614303