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DO Term : iridogoniodysgenesis syndrome [DOID:0050786] Disease Ontology

Namespace  disease_ontology Obsolete  false
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 dominant inheritance of mutations in the PITX2 gene.
  • synonyms:
  • iridogoniodysgenesis type 2,
  • 601631,
  • IRID 2,
  • GARD:3026,
  • OMIM:601631,
  • 137600,
  • IGDS,
  • OMIM:137600,
  • ORDO:98634,
  • IRID 1,
  • iridogoniodysgenesis type 1
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents