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Disease Ontology Browser
iridogoniodysgenesis syndrome (DOID:0050786)
Synonyms: IGDS; IRID 1; IRID 2; iridogoniodysgenesis type 1; iridogoniodysgenesis type 2
Alt IDs: OMIM:137600, OMIM:601631, ORDO:98634
Definition: An autosomal dominant 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.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
06/20/2017
MGI 6.10
The Jackson Laboratory