Noonan syndrome 8

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Summary

Literature (0)

DOID:0060586 - Noonan syndrome 8

Disease Ontology Definition:A Noonan syndrome that has_material_basis_in caused by heterozygous mutation in the RIT1 gene on chromosome 1q22.

Synonyms: NS8

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

: rit1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014143 - Noonan syndrome 8

MONDO:0014143 - Noonan syndrome 8

MIM:

MIM:615355 - NOONAN SYNDROME 8; NS8

MIM:615355 - NOONAN SYNDROME 8; NS8

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)