Rieger anomaly

Axenfeld–Rieger syndrome is a rare autosomal dominant disorder, which affects the development of the teeth, eyes, and abdominal region. Pathophysiology The molecular genetics of Axenfeld–Rieger syndrome are poorly understood, but center on three genes identified by cloning of chromosomal breakpoints from patients.This disorder is inheritable as an autosomal dominant trait, which means the defective gene is located on an autosome, and only one copy of the gene is sufficient to cause the disorder when inherited from a parent who has the disorder. [Source: Wikipedia ]

OrphaNet reference
Rieger anomaly 
Is A
Mesodermal dysplasia
May Be Caused by
Rieger syndrome
SHORT syndrome