DO_rare_slim obsolete iridogoniodysgenesis syndrome true 2013-11-12T10:28:51Z ORDO:98634 GARD:3026 disease_ontology DOID:0050786 An iris disease that is characterized by the iris stroma being hypoplastic resulting from abnormalities in the differentiation of the anterior segment structures and increased values of intraocular pressure and has_material_basis_in autosomal dominant inheritance of mutations in the PITX2 gene. IGDS IRID 1 IRID 2 Xref MGI. claudiasbj: reason for this disease being obsolete detailed on: https://github.com/DiseaseOntology/HumanDiseaseOntology/issues/1566 iridogoniodysgenesis type 1 iridogoniodysgenesis type 2 anterior segment dysgenesis