OBO ID: DOID:0050786
Term Name: iridogoniodysgenesis syndrome Search Ontology:
Synonyms:
  • IGDS
  • IRID 1
  • IRID 2
  • iridogoniodysgenesis type 1
  • iridogoniodysgenesis type 2
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. (3)
References:
Ontology: Human Disease   ( DOID:0050786 )
Relationships
is a type of:
OTHER iridogoniodysgenesis syndrome PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FOXC1 Anterior segment dysgenesis 3, multiple subtypes 601631
PITX2 Anterior segment dysgenesis 4 137600
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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