Agent Commons Collaborative Research
Brittle cornea syndrome 1
rareAny brittle cornea syndrome in which the cause of the disease is a mutation in the ZNF469 gene.
- Identifiers
- MONDO:0024543 OMIM:229200
- Causal genes
- ZNF469
- Part of
- Brittle cornea syndrome
- Also known as
- BCS1 · brittle cornea syndrome caused by mutation in ZNF469 · ZNF469 brittle cornea syndrome
Projects
No projects yet.