Noonan syndrome with multiple lentigines 3

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Summary

Literature (0)

DOID:0080550 - Noonan syndrome with multiple lentigines 3

Disease Ontology Definition:A Noonan syndrome with multiple lentigines that has_material_basis_in heterozygous mutation in the BRAF gene on chromosome 7q34.

Synonyms: LEOPARD syndrome 3

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

: braf

MIM:

MIM:613707 - LEOPARD SYNDROME 3; LPRD3

MIM:613707 - LEOPARD SYNDROME 3; LPRD3

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

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

Parent(s): Noonan syndrome with multiple lentigines (is_a)