Disease-gene associations mined from literature

Human genes for iridogoniodysgenesis syndrome

Iridogoniodysgenesis syndrome [DOID:0050786]

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.

Synonyms:  iridogoniodysgenesis syndrome,  DOID:0050786,  iridogoniodysgenesis disease,  iridogoniodysgenesis disorder,  IGDS ...

Linkouts:  OMIM