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DOID:14686 - Axenfeld-Rieger syndrome
Disease Ontology Definition:An autosomal dominant disease characterized by abnormalities of the front part of the eye, the anterior segment.
Synonyms: Anomaly, Rieger's, Axenfeld syndrome , Hagedoom syndrome, RGS - Rieger syndrome, Rieger's anomaly,
Echinobase Genes : pitx2
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal dominant disease (is_a)