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:608837 - CARNEY COMPLEX VARIANT

Xenbase Genes: myh8

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012137 - Carney complex - trismus - pseudocamptodactyly syndrome

Disease Ontology (DO):
DOID:0050471 - Carney complex