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chromosome 17p13.3 duplication syndrome (DOID:0060432)
Alliance: disease page
Synonyms: 17p13.3 duplication syndrome; 17p13.3 microduplication syndrome; chromosome 17p13.3 centromeric duplication syndrome; trisomy 17p13.3
Alt IDs: OMIM:613215, ICD10CM:Q92.3, MESH:C567705, ORDO:217385
Definition: A chromosomal duplication syndrome that has_material_basis_in duplication of the chromosome 17p13.3 region.


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
03/19/2024
MGI 6.23
The Jackson Laboratory