has material basis in germline mutation in
MIR184
syndromic disease
hereditary disease
EDICT syndrome
https://github.com/monarch-initiative/mondo/issues/6744
https://github.com/monarch-initiative/mondo/issues/6877
UMLS:C3280392
endothelial dystrophy-iris hypoplasia-congenital cataract-stromal thinning syndrome
EDICT (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.
keratoconus with cataract
keratoconus, familial, with early-onset anterior polar cataract
EDICT
GARD:17349
OMIM:614303
endothelial dystrophy, iris hypoplasia, congenital cataract, and stromal thinning syndrome
Orphanet:293936
EDICT syndrome
MONDO:0013678
autosomal dominant keratoconus with early-onset anterior polar cataracts
KTCNCT
familial keratoconus with cataract
SCTID:722439009