Iridogoniodysgenesis Syndrome
Disease ID: disease_node_17298
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| Dbxref | GARD:3026, MIM:137600, MIM:601631, ORDO:98634 |
|---|---|
| Subclassof | DOID_0050736, DOID_240 |
| Data Source | DOID |
| Synonyms | IGDS, IRID 1, IRID 2, iridogoniodysgenesis type 1, iridogoniodysgenesis type 2 |
| Doid Label | iridogoniodysgenesis syndrome |
| Doid Description | 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 domit inheritance of mutations in the PITX2 gene. Xref MGI. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_17298 |
| Doid Id | DOID_0050786 |
| Label | Iridogoniodysgenesis Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Iris Diseases(ID:disease_node_4348) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)