has characteristic has characteristic iridogoniodysgenesis congenital ectropion uveae https://github.com/monarch-initiative/mondo/issues/4069 https://www.malacards.org/card/congenital_ectropion_uveae UMLS:C1303012 MONDO:0019630 Congenital ectropion uveae is a rare, genetic, non-syndromic developmental defect of the eye characterized by the presence of iris pigment epithelium on the anterior surface of the iris, anterior insertion of the iris, angle dysgenesis and progressive open-angle glaucoma (the latter may present in infancy or may develop later in life). Patients may manifest with headaches, ocular pain, photophobia, and redness, watering and/or swelling of the eye. It can often be associated with neurofibromatosis and less commonly with other ocular abnormalities. Orphanet:91491 GARD:0019169 MEDGEN:724517 congenital