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Iridogoniodysgenesis Syndrome

Disease ID: disease_node_17298

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DbxrefGARD:3026, MIM:137600, MIM:601631, ORDO:98634
SubclassofDOID_0050736, DOID_240
Data SourceDOID
SynonymsIGDS, IRID 1, IRID 2, iridogoniodysgenesis type 1, iridogoniodysgenesis type 2
Doid Labeliridogoniodysgenesis syndrome
Doid DescriptionAn 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 domit inheritance of mutations in the PITX2 gene. Xref MGI.
Has Material Basis InGENO_0000147
Disease Node Iddisease_node_17298
Doid IdDOID_0050786
LabelIridogoniodysgenesis Syndrome