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:615665 - JOUBERT SYNDROME 22; JBTS22

Xenbase Genes: pde6d

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010176 - orofaciodigital syndrome type 6
MONDO:0014297 - Joubert syndrome 22

Disease Ontology (DO):
DOID:0110991 - Joubert syndrome 22