iris disorder hereditary glaucoma anterior segment dysgenesis 3 https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/5789 https://rarediseases.info.nih.gov/diseases/2482/glaucoma-iridogoniodysgenesia https://www.malacards.org/card/anterior_segment_dysgenesis_3 MESH:C535535 iridogoniodysgenesis type 1 iris hypoplasia with glaucoma iridogoniodysgenesis anomaly, autosomal dominant anterior segment dysgenesis 3, multiple subtypes IGDA syndrome MONDO:0024456 Editor note: check GARD re 2482 FOXC1 iridogoniodysgenesis DOID:0080608 GARD:0002978 glaucoma iridogoniodysplasia, familial OMIM:601631 ASGD3 IGDA glaucoma iridogoniodysgenesia iridogoniodysgenesis caused by mutation in FOXC1 An iridogoniodysgenesis that results from alterations in the forkhead transcription factor gene (FOXC1) anterior segment dysgenesis 3 UMLS:C5975707 iridogoniodysgenesis, type 1 MEDGEN:1875235 IRID1 FOXC1-related anterior segment dysgenesis