Axenfeld-Rieger syndrome type 3

Definition

Any Axenfeld-Rieger syndrome in which the cause of the disease is a mutation in the FOXC1 gene.

Also known as anterior chamber cleavage syndrome, Axenfeld-Rieger syndrome caused by mutation in FOXC1, Axenfeld-Rieger syndrome type 3, FOXC1 Axenfeld-Rieger syndrome, RIEG3 — per MONDO

Also identified as

• DOID 0110122 per MONDO
• ICD9 743.44 per MONDO
• OMIM 602482 per MONDO
• SCTID 22155002 per MONDO
• UMLS C2678503 per MONDO