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Disease Ontology Browser
Noonan syndrome 6 (DOID:0060584)
Alliance: disease page
Synonyms: NS6
Alt IDs: OMIM:613224, ICD10CM:Q87.1, MESH:C548084
Definition: A Noonan syndrome that has_material_basis_in heterozygous mutation in the NRAS gene on chromosome 1p13.


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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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory