Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
OMIM:614170 - BRITTLE CORNEA SYNDROME 2; BCS2


Xenbase Genes: prdm5

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013605 - brittle cornea syndrome 2

Disease Ontology (DO):
DOID:14775 - brittle cornea syndrome