You are using an outdated browser. Please upgrade your browser to improve your experience.
iridogoniodysgenesis
Disease Summary
Associated Targets (8)
Tbio
6
Tchem
2
Disease Ontology 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.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0050786
Orphanet:98634
MONDO:0011119
High level summary of knowledge for a disease, including descriptions and datasource references.