- OMIM ID
-
601631
- OMIM term:
- IRIDOGONIODYSGENESIS, TYPE 1; IRID1
- Alternative terms:
-
IRIDOGONIODYSGENESIS ANOMALY, AUTOSOMAL DOMINANT; IGDA IRIS HYPOPLASIA WITH GLAUCOMA, INCLUDED
GLAUCOMA IRIDOGONIODYSPLASIA, FAMILIAL, INCLUDED
- (∗) Location:
- 6p25.3
- (†) Associated OMIM genes:
- FOXC1
- (‡) Associated MGI genes:
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