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)
MIM:616258 - MECKEL SYNDROME 12; MKS12

Xenbase Genes: kif14, kif14l

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014552 - lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome