Axenfeld-Rieger syndrome type 2 Disease Ontology Browser

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Disease Ontology Browser

Axenfeld-Rieger syndrome type 2 (DOID:0110121)
Alliance: disease page
Synonyms: RIEG2; Rieger syndrome type 2
Alt IDs: OMIM:601499, ICD10CM:Q13.8
Definition: An Axenfeld-Rieger syndrome characterized by bnormal development of the anterior segment of the eye, which results in blindness from glaucoma in approximately 50% of affected individuals that has_material_basis_in deletions in the region 13q14.

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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