Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0050786 - iridogoniodysgenesis syndrome

Disease Ontology 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.

Synonyms: IGDS, IRID 1, IRID 2, iridogoniodysgenesis type 1, iridogoniodysgenesis type 2

Xenbase Genes : foxc1, pitx2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011119 - iridogoniodysgenesis


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), iris disease (is_a)