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DOID:3490 - Noonan syndrome
Disease Ontology Definition:A RASopathy that is characterized by mildly unusual facial features, short stature, heart defects, bleeding problems, skeletal malformations, and many other signs and symptoms.
Synonyms: Turner's phenotype, karyotype normal, Turner's phenotype, karyotype normal (disorder),
Echinobase Genes :
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
monogenic disease (is_a),
syndrome (is_a)