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 (1)
DOID:0050469 - Costello syndrome


Disease Ontology Definition:A RASopathy characterized by craniofacial dysmorphology, cardiac defects, mild mental retardation, and high birth weight followed by a failure to thrive and developmental delays.

Synonyms: FCS SYNDROME, Faciocutaneoskeletal Syndrome

In OMIM:
OMIM:218040 - COSTELLO SYNDROME; CSTLO

In Mondo Disease Ontology:
MONDO:0009026 - Costello syndrome

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : hras, kras

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): RASopathy (is_a), autosomal dominant disease (is_a), syndrome (is_a)