FOXC1-related anterior segment dysgenesis
MONDO:0100235Any anterior segment dysgenesis in which the cause of the disease is a mutation in the FOXC1 gene.
2 clinical trials for this condition and its sub-types, 0 tagged with FOXC1-related anterior segment dysgenesis itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Part of
Sub-types of FOXC1-related anterior segment dysgenesis
-
Axenfeld-Rieger syndrome type 3 1 trial
-
Anterior segment dysgenesis 3 1 trial
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.