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Disease Ontology Browser
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 the PAFAH1B1 and/or the YWHAE gene on chromosome 17p13.3.

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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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12/10/2024
MGI 6.24 		The Jackson Laboratory