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Disease Ontology Browser
Axenfeld-Rieger syndrome type 3 (DOID:0110122)
Alliance: disease page
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
Alt IDs: OMIM:602482, ICD10CM:Q13.8
Definition: An Axenfeld-Rieger syndrome that has_material_basis_in heterozygous mutation in the FOXC1 gene on chromosome 6p25.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
11/26/2019
MGI 6.14
The Jackson Laboratory