Noonan syndrome 2

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Summary

Literature (0)

DOID:0060580 - Noonan syndrome 2

Disease Ontology Definition:A Noonan syndrome characterized by hypertrophic obstructive cardiomyopathy and that has_material_basis_in an autosomal recessive inheritance.

Synonyms: NS2,

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

: lztr1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011531 - Noonan syndrome 2

MONDO:0011531 - Noonan syndrome 2

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): Noonan syndrome (is_a), autosomal recessive disease (is_a)