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General Information
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| Term |
iridogoniodysgenesis syndrome |
ID (Ontology) |
DOID:0050786 (Human Disease) |
| Definition |
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. |
| Also Known As |
"IGDS" ; "IRID 1" ; "IRID 2" (for all, see Synonyms field below) |
| Comment |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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No relevant records available
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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| Full annotation statements | Relevant FlyBase reports |
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| Genes |
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iridogoniodysgenesis syndrome | 2 | for disease ribbon | iridogoniodysgenesis syndrome | 2 | model of | iridogoniodysgenesis syndrome | 2 |
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Relationships