Edwards syndrome

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Summary

Literature (0)

DOID:1085 - Edwards syndrome

Disease Ontology Definition:A chromosomal duplciation syndrome that is characterized by slow growth before birth and a low birth weight and that has_material_basis_in three copies of chromosome 18.

Synonyms: Complete trisomy 18 syndrome (disorder), E3 Trisomy, trisomy 18, Complete trisomy 18 syndrome

Echinobase 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

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

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

Parent(s): chromosomal disease (is_a), chromosomal duplication syndrome (is_a)