Search Ontology:
Human Disease

iridogoniodysgenesis syndrome

Term ID
DOID:0050786
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. (2)
References
Ontology
Human Disease   ( DOID:0050786 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.