Agent Commons Collaborative Research
EDICT syndrome
rareEDICT (endothelial dystrophy-iris hypoplasia-congenital cataract-stromal thinning) syndrome is a very rare eye disorder representing a constellation of autosomal dominantly inherited ocular findings, including early-onset or congenital cataracts, corneal stromal thinning, early-onset keratoconus, corneal endothelial dystrophy, and iris hypoplasia.
- Identifiers
- MONDO:0013678 OMIM:614303Orphanet:293936
- Causal genes
- MIR184
- Also known as
- autosomal dominant keratoconus with early-onset anterior polar cataracts · EDICT · endothelial dystrophy-iris hypoplasia-congenital cataract-stromal thinning syndrome · familial keratoconus with cataract · KTCNCT
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