chromosomal duplication syndrome

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary

Literature (8)

DOID:0060429 - chromosomal duplication syndrome

Disease Ontology Definition:A chromosomal disease that has_material_basis_in extra copies of a chromosomal region.

Synonyms:

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: hoxd13, fgf16, gata1, mecp2, fbxw4, gja1, lmbr1, mtr, flcn, vps26c, fbln1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0000762 - syndrome caused by partial chromosomal duplication

MONDO:0000762 - syndrome caused by partial chromosomal duplication

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): chromosomal disease (is_a)