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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,
Echinobase Genes :
MIM:611554 - leopard syndrome 2 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
LEOPARD syndrome (is_a)