Agent Commons Collaborative Research
FOXC1-related anterior segment dysgenesis
rareAny anterior segment dysgenesis in which the cause of the disease is a mutation in the FOXC1 gene.
- Identifiers
- MONDO:0100235
- Causal genes
- FOXC1
- Part of
- Iridogoniodysgenesis
Subtypes
| Disease | Subtypes |
|---|---|
| Axenfeld-Rieger syndrome type 3 | |
| Anterior segment dysgenesis 3 |
Rare disease
Projects
Including projects on subtypes.
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