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ENAnterior Segment Dysgenesis 3 (ASGD3)
Alias:
Iridogoniodysgenesis, Type 1
Iridogoniodysgenesis Anomaly, Autosomal Dominant
Glaucoma Iridogoniodysplasia, Familial
Iris Hypoplasia with Glaucoma
Irid1
Anterior Segment Dysgenesis 3, Multiple Subtypes
Asgd3
Igda
Iridogoniodysgenesis Anomaly
Igda Syndrome
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Anterior Segment Dysgenesis 3, also known as iridogoniodysgenesis, type 1, is related to primary congenital glaucoma and iris hypoplasia with glaucoma. An important gene associated with Anterior Segment Dysgenesis 3 is FOXC1 (Forkhead Box C1). Affiliated tissues include eye and skin, and related phenotypes are cerebellar vermis hypoplasia and enlarged cisterna magna
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