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Summary Literature (0)
DOID:0060578 - Noonan syndrome 1

Disease Ontology Definition:A Noonan syndrome that has_material_basis_in the PTPN11 gene on chromosome 12q24.

Synonyms: NS1

Xenbase Genes : map2k1, braf, ptpn11

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008104 - Noonan syndrome 1

MIM:
MIM:163950 - NOONAN SYNDROME 1; NS1

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

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