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Axenfeld-Rieger syndrome type 2

MONDO:0011097

An Axenfeld-Rieger syndrome that has material basis in deletions in the region 13q14.

Also known as: RIEG2, Axenfeld-Rieger syndrome, type 2, Rieger syndrome, type 2

13 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Hereditary disease (172) Eye disorder (97) Syndromic disease (24) Human disease (14) Developmental defect during embryogenesis (7) Disorder of orbital region (3) Disease of genetic or genomic mechanism (2) Axenfeld-Rieger syndrome (1) Disorder of visual system (1)
Trials to join now! 9 Not yet finished but already full! 1 Completed 2 Terminated 1
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