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Disease Ontology Browser
iridogoniodysgenesis syndrome (DOID:0050786)
Alliance: disease page
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 Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
MGI 6.14
The Jackson Laboratory