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Summary Literature (0)
DOID:0110122 - Axenfeld-Rieger syndrome type 3


Disease Ontology Definition:An Axenfeld-Rieger syndrome that has material basis in heterozygous mutation in the FOXC1 gene on chromosome 6p25.

Synonyms: Axenfeld-Rieger anomaly with or without cardiac defects and/or sensorineural hearing loss, RIEG3, Rieger syndrome type 3, anterior chamber cleavage syndrome, anterior segment mesenchymal dysgenesis


In Mondo Disease Ontology:
MONDO:0011233 - Axenfeld-Rieger syndrome type 3

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : foxc1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): Axenfeld-Rieger syndrome (is_a)