FOXC1
MIM.601090 6p25
Pathology
germline mutations in
- anterior segment anomalies
- iridogoniodysgenesis type 1 (MIM.601631)
- Rieger anomaly (with dental and facial abnormalities)
- Axenfeld anomaly
- Peters anomaly
- iris anomalies
- iris hypoplasia
- glaucoma
- isolated posterior embryotoxon