iridogoniodysgenesis syndrome (DOID:0050786)
Alliance: disease page
Synonyms: IGDS; IRID 1; IRID 2; iridogoniodysgenesis type 1; iridogoniodysgenesis type 2
Alt IDs: OMIM:137600, OMIM:601631, ORDO:98634
Definition: 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.