obsolete iridogoniodysgenesis syndrome

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 inherita

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.

Also known as: IGDS; IRID 1; IRID 2; iridogoniodysgenesis type 1; iridogoniodysgenesis type 2