All diseases

OMIM ID
137600
OMIM term:
IRIDOGONIODYSGENESIS, TYPE 2; IRID2
Alternative terms:
IRIDOGONIODYSGENESIS SYNDROME; IGDS
IRIS HYPOPLASIA WITH EARLY-ONSET GLAUCOMA, AUTOSOMAL DOMINANT; IHGA
(∗) Location:
4q25  
(†) Associated OMIM genes:
PITX2  
(‡) Associated MGI genes:

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