Axenfeld-Rieger syndrome type 2

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Summary

Literature (0)

DOID:0110121 - Axenfeld-Rieger syndrome type 2

Disease Ontology Definition:An Axenfeld-Rieger syndrome that has_material_basis_in deletions in the region 13q14.

Synonyms: RIEG2, Rieger syndrome type 2

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): Axenfeld-Rieger syndrome (is_a), chromosomal deletion syndrome (is_a)