All diseases

OMIM ID
602482
OMIM term:
AXENFELD-RIEGER SYNDROME, TYPE 3; RIEG3
Alternative terms:
AXENFELD-RIEGER ANOMALY WITH OR WITHOUT CARDIAC DEFECTS AND/OR SENSORINEURAL HEARING LOSS
ANTERIOR SEGMENT MESENCHYMAL DYSGENESIS
ANTERIOR CHAMBER CLEAVAGE SYNDROME
RIEGER SYNDROME, TYPE 3 AXENFELD ANOMALY, INCLUDED
RIEGER ANOMALY, INCLUDED
AXENFELD-RIEGER ANOMALY, INCLUDED
(∗) Location:
6p25.3  
(†) Associated OMIM genes:
FOXC1  
(‡) Associated MGI genes:
Bmp4  

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