iridogoniodysgenesis, type 2 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description 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. (Human Disease Ontology, DOID_0050786)
External Link http://www.omim.org/entry/137600
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Genes

1 genes associated with the iridogoniodysgenesis, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
PITX2 paired-like homeodomain 2