Noonan syndrome with multiple lentigines 2

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Summary

Literature (0)

DOID:0080549 - Noonan syndrome with multiple lentigines 2

Disease Ontology Definition:A Noonan syndrome with multiple lentigines that has_material_basis_in heterozygous mutation in the RAF1 gene on chromosome 3p25.

Synonyms: LEOPARD syndrome 2

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

: raf1

MIM:

MIM:611554 - LEOPARD SYNDROME 2; LPRD2

MIM:611554 - LEOPARD SYNDROME 2; LPRD2

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)