Any anterior segment dysgenesis in which the cause of the disease is a mutation in the FOXC1 gene.
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congenital microcoria
MONDO:0007989
aniridia-cerebellar ataxia-intellectual disability syndrome
MONDO:0008795
Axenfeld-Rieger syndrome type 3
MONDO:0011233
chromosome 6pter-p24 deletion syndrome
MONDO:0012948
bilateral acute depigmentation of the iris
MONDO:0019074
Rieger anomaly
MONDO:0019628