Axenfeld-Rieger syndrome type 1

MONDO:0008386

A rare autosomal dominant syndrome linked to mutations in the PITX2 gene. It is characterized by abnormalities in the anterior chamber of the eye and underdevelopment of the teeth.

Also known as: Axenfeld-Rieger syndrome caused by mutation in PITX2, Axenfeld-Rieger syndrome type 1, PITX2 Axenfeld-Rieger syndrome, RIEG1, Rieger syndrome type 1, Axenfeld-Rieger syndrome, type 1, Rgs, Rieg

0 clinical trials for this condition and its sub-types, 0 tagged with Axenfeld-Rieger syndrome type 1 itself.

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