Noonan syndrome 6

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Summary

Literature (0)

DOID:0060584 - Noonan syndrome 6

Disease Ontology Definition:A Noonan syndrome that has_material_basis_in heterozygous mutation in the NRAS gene on chromosome 1p13.

Synonyms: NS6

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: nras

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013186 - Noonan syndrome 6

MONDO:0013186 - Noonan syndrome 6

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)