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:300963 - RITSCHER-SCHINZEL SYNDROME 2; RTSC2

Xenbase Genes: ccdc22

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010499 - Ritscher-Schinzel syndrome 2
MONDO:0019078 - Ritscher-Schinzel syndrome

Disease Ontology (DO):
DOID:0060572 - Ritscher-Schinzel syndrome 2