DISEASES

Disease-gene associations mined from literature

Human genes for Axenfeld-Rieger syndrome

Axenfeld-Rieger syndrome [DOID:14686]

An autosomal dominant disease characterized by abnormalities of the front part of the eye, the anterior segment.

Synonyms:  Axenfeld-Rieger syndrome,  AxenfeldRieger syndrome,  Axenfeld-Rieger disease,  Axenfeld-Rieger disorder,  DOID:14686 ...

Linkouts:  OMIM #1 #2 #3