DISEASES

Disease-gene associations mined from literature

Human genes for Axenfeld-Rieger syndrome

Axenfeld-Rieger syndrome [DOID:14686]

Axenfeld syndrome (also known as Axenfeld-Rieger syndrome or Hagedoom syndrome) is the name given to a rare autosomal dominant disorder, which affects the development of the teeth, eyes, and abdominal region.

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