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Echinobase
Summary Literature (0)
DOID:0050469 - Costello syndrome

Disease Ontology Definition:A syndrome 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,

Echinobase Genes :


OMIM:
MIM:218040 - costello syndrome; cstlo

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a)