All diseases

OMIM ID
180500
OMIM term:
AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1
Alternative terms:
RIEGER SYNDROME, TYPE 1
RIEG
RGS
(∗) Location:
4q25  
(†) Associated OMIM genes:
PITX2  
(‡) Associated MGI genes:
Pitx2  

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