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.
Follow this condition — get notified about new trialsSub-types
Broader categories
Disease
(680)
Hereditary disease
(176)
Eye disorder
(102)
Human disease
(14)
Disorder of orbital region
(3)
Anterior segment dysgenesis
(2)
Disease of genetic or genomic mechanism
(2)
Disorder of visual system
(1)
Disease by body system or component
(0)
Disease by developmental or physiological process
(0)