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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 :
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)