Human genes for iridogoniodysgenesis syndrome
Iridogoniodysgenesis syndrome [DOID:0050786]
An 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 dominant inheritance of mutations in the PITX2 gene.
Synonyms: iridogoniodysgenesis syndrome, DOID:0050786, iridogoniodysgenesis disease, iridogoniodysgenesis disorder, iridogoniodysgenesis syndromes ...
Linkouts: OMIM