Term Name:	iridogoniodysgenesis syndrome
Synonyms:	IGDS, IRID 1, IRID 2, iridogoniodysgenesis type 1, iridogoniodysgenesis type 2
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.
Ontology:	Human Disease [DOID:0050786]   ( DOID:0050786 )