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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: anterior chamber cleavage syndrome, anterior segment mesenchymal dysgenesis, Axenfeld-Rieger anomaly with or without cardiac defects and/or sensorineural hearing loss, RIEG3, Rieger syndrome type 3
Xenbase Genes
:
foxc1
| MONDO:0011233 - Axenfeld-Rieger syndrome type 3 |
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)