Brittle cornea syndrome 1

Any brittle cornea syndrome in which the cause of the disease is a mutation in the ZNF469 gene.

Also known as: ZNF469 brittle cornea syndrome, brittle cornea syndrome 1, brittle cornea syndrome caused by mutation in ZNF469, BCS1, Ehlers-Danlos syndrome, type Vib, Ehlers-Danlos syndrome, type Vib, formerly, Fragilitas oculi with Joint hyperextensibility, corneal fragility, keratoglobus, blue sclerae, Joint hyperextensibility

30 clinical trials for this condition and its sub-types.