Noonan syndrome with multiple lentigines 2 Disease Ontology Browser

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Disease Ontology Browser

Noonan syndrome with multiple lentigines 2 (DOID:0080549)
Alliance: disease page
Synonyms: LEOPARD syndrome 2
Alt IDs: OMIM:611554, MESH:C537117
Definition: A Noonan syndrome with multiple lentigines that has_material_basis_in heterozygous mutation in the RAF1 gene on chromosome 3p25.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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