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Noonan syndrome 6 (DOID:0060584)
Alliance: disease page
Synonyms: NS6
Alt IDs: OMIM:613224, DOID:0070106, DOID:0070106, DOID:0070106, DOID:0070106, DOID:0070106, DOID:0070106, DOID:0070106, DOID:0070106, DOID:0070106, DOID:0070106, DOID:0070106, DOID:0070106, DOID:0070106, DOID:0070106, DOID:0070106, ICD10CM:Q87.1
Definition: A Noonan syndrome that has_material_basis in heterozygous mutation in the NRAS gene on chromosome 1p13.


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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/04/2018
MGI 6.13
The Jackson Laboratory